- Reference #:
Recipient NameMs. Refiye Adiyaman
Recipient TitleManager, Quality Operations Group
- Deva Holding AS - Cerkezkoy Subesi
Halkalı Merkez Mah. Basın Expres Caddesi No:1
- Issuing Office:
- Center for Drug Evaluation and Research | CDER
Dear Ms. Adiyaman,
The Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our Warning Letter 320-19-33 dated August 6, 2019.
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 and/or deviations be observed during a subsequent inspection or through other means.
for Joan Johnson
Division of Drug Quality I