FDA Letter API

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 More Warning Letters Warning Letters About Warning and Close-Out Letters 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