FDA Letter API

Malladi Drugs & Pharmaceuticals Ltd.

Letter data

Company
Malladi Drugs & Pharmaceuticals Ltd.
Recipient
Mr. V.N. Gopalkrishnan | Co-Founder & Chairman | Malladi Drugs & Pharmaceuticals Ltd. | SKCL Tech Square, 7th Floor, Plot No.: South Phase 14 | Thiru Vi Ka Industrial Estate | Guindy, Chennai | 600032 | Tamil Nadu | India
Issue date
2023-01-31
Posted date
Not available
FDA office
Center for Drug Evaluation and Research | CDER
Subject
Not available
Product
Drugs
CMS ID
541915
Reference number
3005115135
FEI
Not available
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 Malladi Drugs & Pharmaceuticals Ltd. MARCS-CMS 541915 — January 31, 2023 More Warning Letters Warning Letters About Warning and Close-Out Letters Reference #: 3005115135 Product: Drugs Recipient: Recipient Name Mr. V.N. Gopalkrishnan Recipient Title Co-Founder & Chairman Malladi Drugs & Pharmaceuticals Ltd. SKCL Tech Square, 7th Floor, Plot No.: South Phase 14 Thiru Vi Ka Industrial Estate Guindy, Chennai 600032 Tamil Nadu India Issuing Office: Center for Drug Evaluation and Research | CDER United States Dear Mr. Gopalkrishnan: The Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our Warning Letter 320-18-40 dated March 09, 2018. Based on our evaluation, it appears that you have addressed the deviations 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 deviations be observed during a subsequent inspection or through other means. Sincerely, /S/ Frank Wackes Compliance Officer Division of Drug Quality II Content current as of: 02/03/2023 Regulated Product(s) Drugs