FDA Letter API

LNK International, Inc.

Letter data

Company
LNK International, Inc.
Recipient
Mr. Pankaj S. Chudgar | President | LNK International, Inc. | 22 Arkay Dr | Hauppauge | , | NY | 11788 | United States
Issue date
2021-12-01
Posted date
Not available
FDA office
Division of Pharmaceutical Quality Operations I
Subject
Not available
Product
Drugs
CMS ID
582253
Reference number
Not available
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 LNK International, Inc. MARCS-CMS 582253 — December 01, 2021 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: READ/DELIVERY RECEIPT Product: Drugs Recipient: Recipient Name Mr. Pankaj S. Chudgar Recipient Title President LNK International, Inc. 22 Arkay Dr Hauppauge , NY 11788 United States Issuing Office: Division of Pharmaceutical Quality Operations I United States Dear Mr. Chudgar: The U.S. Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our Warning Letter [CMS #582253], dated September 26, 2019. Based on our evaluation, it appears that you have adequately addressed the violations contained in this Warning Letter. 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 Agency 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. Respectfully, /S/ Diana Amador-Toro Program Division Director/District Director U.S. Food and Drug Administration OPQO Division I / New Jersey District Content current as of: 12/14/2021 Regulated Product(s) Drugs