FDA Letter API

Delta Kozmetik Sanayi Ve Ticaret-Selim Yesil

Letter data

Company
Delta Kozmetik Sanayi Ve Ticaret-Selim Yesil
Recipient
Ms.Gulten Erdemir | General Manager | Delta Kozmetik Sanayi Ve Ticaret-Selim Yesil | Bolgesi Aydinli Sb Mahallesi | 6 12 Istanbul Endustri Veticaret Serbest | 34953 | Sokak Tuzla | / | İstanbul | Turkey
Issue date
2026-06-05
Posted date
Not available
FDA office
Center for Drug Evaluation and Research (CDER)
Subject
Not available
Product
Drugs
CMS ID
614402
Reference number
Not available
FEI
3010166780
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 Delta Kozmetik Sanayi Ve Ticaret-Selim Yesil MARCS-CMS 614402 — June 05, 2026 More Warning Letters Warning Letters About Warning and Close-Out Letters Reference #: FEI 3010166780 Product: Drugs Recipient: Recipient Name Ms.Gulten Erdemir Recipient Title General Manager Delta Kozmetik Sanayi Ve Ticaret-Selim Yesil Bolgesi Aydinli Sb Mahallesi 6 12 Istanbul Endustri Veticaret Serbest 34953 Sokak Tuzla / İstanbul Turkey Issuing Office: Center for Drug Evaluation and Research (CDER) United States Secondary Issuing Offices United States Dear Ms. Erdemir: The Food and Drug Administration (FDA) has completed an evaluation of your firm’s corrective actions in response to our Warning Letter 320-23-11 dated February 13, 2023, and Warning Letter 320-21-51 dated July 8, 2021. 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/ Bryce Hammer Compliance Officer Division of Drug Quality II Content current as of: 06/09/2026 Regulated Product(s) Drugs