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
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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