The Skin Atelier, Inc
FDA inspection history in Goshen, New York, 2019 to 2024
- 2
- Close-outs
- 1
- Form 483
Every document, by year
- Close-out
- Form 483
2019: one close-out letter and one Form 483; 2024: one close-out letter.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One close-out letter and one Form 483, at Goshen, New York.
- 2024One close-out letter, at Goshen, New York.
Cited most
Across all The Skin Atelier observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.113(a)Control of microbiological contamination1
- 21 CFR 211.125(f)Labeling issuance1
- 21 CFR 211.137(b)Expiration dating1
- 21 CFR 211.165(a)Testing and release for distribution1
The complete The Skin Atelier file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Goshen, New York
Two close-out letters and one Form 483 · 2019 to 2024 · 9 observations
Latest: Close-out, Oct 29, 2024 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-10-29 | Close-out Close-out letter | Goshen, New York | — | $99 |
| 2019-10-01 | Close-out Close-out letter | Goshen, New York | — | $99 |
| 2019-04-04 | 483 Form 483 | Goshen, New York | 9 | $99 |
Investigators on these documents
FEI number 3005976760 · most recent document Oct 29, 2024
About The Skin Atelier, Inc
How many FDA Form 483s has The Skin Atelier, Inc received?
FDA Intel has 1 Form 483 on file for The Skin Atelier, Inc; the most recent is dated Apr 4, 2019.
When was The Skin Atelier, Inc last inspected by FDA?
The most recent FDA inspection document on file for The Skin Atelier, Inc is a Form 483 dated Apr 4, 2019, for the site in Goshen, New York.
What did FDA cite at The Skin Atelier, Inc?
The regulations cited most in the observations on file for The Skin Atelier, Inc are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.113(a) (Control of microbiological contamination), 1 time; 21 CFR 211.125(f) (Labeling issuance), 1 time.