Colorlab Cosmetics, Inc.
FDA inspection history in Williston, Vermont, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Williston, Vermont.
Cited most
Across all Colorlab Cosmetics observations on file
- 21 CFR 211.22(a)Responsibilities of quality control unit1
The complete Colorlab Cosmetics file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Williston, Vermont
One Form 483 · 2022 · 2 observations
Latest: Form 483, Jan 6, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-01-06 | 483 Form 483 | Williston, Vermont | 2 | $99 |
Investigators on these documents
FEI number 3005000375 · most recent document Jan 6, 2022
About Colorlab Cosmetics, Inc.
How many FDA Form 483s has Colorlab Cosmetics, Inc. received?
FDA Intel has 1 Form 483 on file for Colorlab Cosmetics, Inc.; the most recent is dated Jan 6, 2022.
When was Colorlab Cosmetics, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Colorlab Cosmetics, Inc. is a Form 483 dated Jan 6, 2022, for the site in Williston, Vermont.
What did FDA cite at Colorlab Cosmetics, Inc.?
The regulations cited most in the observations on file for Colorlab Cosmetics, Inc. are 21 CFR 211.22(a) (Responsibilities of quality control unit), 1 time.