NSEGeneral Updates3d ago · 18 Sept 2026, 06:59 pm
General Updates
Shilpa Medicare Limited · SHILPAMED
✦ AI SummaryRegulatory
Shilpa Medicare Limited has informed the Exchange about USFDA Inspection of Shilpa Medicare Limited, Unit VII, Analytical Services Division, Hyderabad. The inspection concluded with one procedural observation, which was neither a repeat observation nor related to data integrity.
Analysis Scores
Earnings Impact5/10
Growth Catalyst2/10
Governance Concern1/10
Regulatory Risk6/10
Balance Sheet Risk1/10
Liquidity Impact8/10
Market Sentiment5/10
✦ Ask a Question
Ask anything about this announcement — AI will answer based on the filing content.
Full Announcement
Shilpa Medicare Limited has informed the Exchange about USFDA Inspection of Shilpa Medicare Limited, Unit VII, Analytical Services Division, Hyderabad.
Attachments (1)
📄pdf
Download →
SHILPAMED_18092026185924_Intimation_on_USFDA.pdf
View document text
Shilpa Medicare Limited
Corporate & Admin Office:
“Shilpa House”, # 12-6-214/A-1, Hyderabad Road,
Raichur – 584 135, Karnataka, India
Tel: +91-8532-238704, Fax: +91-8532-238876
Email: info@vbshilpa.com, Web: www.vbshilpa.com
CIN: L85110KA1987PLC008739
Date: 18 September 2026
Corporate relationship Department, National Stock Exchange of India, Limited
BSE Limited, Exchange Plaza, 5th Floor,
1st Floor, Rotunda Building Plot No. C/1, G Block, Bandra-Kurla Complex,
P.J Towers Dalal Street, Fort, Bandra (E),
Mumbai 400001 Mumbai 400051
Stock Code: BSE – 530549 / NSE – SHILPAMED
Dear Sir/Ma’am,
SUB: USFDA Inspection of Shilpa Medicare Limited, Unit VII, Analytical Services Division, Hyderabad.
REF: Intimation under regulation 30 of SEBI (LODR) Regulations 2015.
This is to notify that the USFDA conducted Surveillance Inspection at Unit VII of Shilpa Medicare Limited,
Analytical Services Division situated at Plot No.79, Road No. 15, Survey No.125, IDA Mallapur, Nacharam, Uppal
Mandal, Medchal, Malkajgiri Dist. – 500076 Hyderabad, Telangana from 16 September 2026 to 18 September
2026. The inspection concluded with one procedural observation, which was neither a repeat observation nor
related to data integrity. The Company will address the observation and respond within stipulated timeline.
The details of the above Inspection (as required to be furnished pursuant to Regulation 30 read with Para A
of Part A of Schedule III of SEBI Listing Regulations and SEBI Circular No. SEBI/HO/49/14/14(7)2025-CFD-
POD2/I/3762/2026 dated 30th January 2026) are enclosed as Annexure A.
The above information is also available on the website of the Company www.vbshilpa.com
For SHILPA MEDICARE LIMITED
Ritu Tiwary
Company Secretary & Compliance Officer
Shilpa Medicare Limited
Corporate & Admin Office:
“Shilpa House”, # 12-6-214/A-1, Hyderabad Road,
Raichur – 584 135, Karnataka, India
Tel: +91-8532-238704, Fax: +91-8532-238876
Email: info@vbshilpa.com, Web: www.vbshilpa.com
CIN: L85110KA1987PLC008739
Annexure A
Disclosure of events and information pursuant to Regulation 30 of SEBI (Listing Obligations and Disclosure
Requirements) Regulations, 2015 read with Master Circular No. HO/49/14/14(7)2025-CFDPOD2/I/3762/2026
dated 30th January 2026.
Sr. No. Particulars Details
1. Name of the authority United States Food and Drug Administration (US
FDA), USA
2. Nature and details of the action(s) taken, The United States Food and Drug Administration
initiated or order(s) passed by the Authority (USFDA) has conducted a Surveillance Inspection
(SI) at Analytical Services Division located at
Hyderabad.
The inspection was completed on 18 September
2026. At the conclusion of the inspection, the
USFDA issued one observation, which was
procedural in nature.
3. Date of receipt of direction or order, including 18 September 2026
any ad-interim or interim orders, or any other
communication from the authority
4. Details of the violation(s)/ contravention(s) The inspection was completed on 18 September
committed or alleged to be committed 2026. At the conclusion of the inspection, the
USFDA issued one observation, which was
procedural in nature.
We will submit a comprehensive response to the
USFDA within the stipulated timeline, addressing
the observation with appropriate corrective and
preventive actions. The Company is committed to
maintaining the highest standards of quality and
compliance across all its operations.
5 Impact on financial, operation or other We do not expect this development to have any
activities of the listed entity, quantifiable in material impact on the current business
monetary terms to the extent possible operations or existing supplies from this facility.