Zydus Lifesciences Limited
Letter data
- Company
- Zydus Lifesciences Limited
- Recipient
- Dr. Sharvil Patel | Managing Director | Zydus Lifesciences Limited | Zydus Corporate Park, S.G. Highway | Nr. Vashnodevi Circle | Ahmedabad | 382482 | India
- Issue date
- 2025-12-09
- Posted date
- Not available
- FDA office
- United States
- Subject
- Not available
- Product
- Drugs
- CMS ID
- 685224
- Reference number
- Not available
- FEI
- 3013712903
- Inspection dates
- Not available
Normalized citations
21 CFR: None found
21 U.S.C.: None found
Related FDA links
No related FDA letter link is present in the source index.
Full source text
CLOSEOUT LETTER
Zydus Lifesciences Limited
MARCS-CMS 685224 —
December 09, 2025
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Reference #:
FEI 3013712903
Product:
Drugs
Recipient:
Recipient Name
Dr. Sharvil Patel
Recipient Title
Managing Director
Zydus Lifesciences Limited
Zydus Corporate Park, S.G. Highway
Nr. Vashnodevi Circle
Ahmedabad
382482
India
Issuing Office:
United States
Secondary Issuing Offices
United States
Dear Mr. Patel:
The Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our Warning Letter 320-24-58 dated August 29, 2024.
Based on our evaluation, it appears that you have addressed the violations contained in this Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of these corrections.
This letter does not relieve you or your firm from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority.
The FDA expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means.
Sincerely,
/S/
Kevin Maguire
Consumer Safety Officer
Division of Drug Quality III
Content current as of:
12/16/2025
Regulated Product(s)
Drugs