Revlon, Inc.
FDA inspection history in Oxford, North Carolina, 2024 to 2026
- 1
- Warning letter
- 1
- Form 483
Every document, by year
- Warning letter
- Form 483
2024: one Form 483; 2026: one warning letter.
The story so far
Built from the dates and citations on the documents themselves.
- 2024–26One Form 483 and one warning letter, at Oxford, North Carolina.
Cited most
Across all Revlon observations on file
- 21 CFR 211.130(e)Packaging and labeling operations1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.67(a)Equipment cleaning and maintenance1
The complete Revlon file.
All 2 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
Oxford, North Carolina
One warning letter and one Form 483 · 2024 to 2026 · 3 observations
Latest: Warning letter, Jun 2, 2026 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-06-02 | Warning letter Warning letter | Oxford, North Carolina | — | $99 |
| 2024-01-12 | 483 Form 483 | Oxford, North Carolina | 3 | $99 |
Investigators on these documents
FEI number 1021184 · most recent document Jun 2, 2026
About Revlon, Inc.
How many FDA Form 483s has Revlon, Inc. received?
FDA Intel has 1 Form 483 on file for Revlon, Inc.; the most recent is dated Jan 12, 2024.
When was Revlon, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Revlon, Inc. is a Form 483 dated Jan 12, 2024, for the site in Oxford, North Carolina.
What did FDA cite at Revlon, Inc.?
The regulations cited most in the observations on file for Revlon, Inc. are 21 CFR 211.130(e) (Packaging and labeling operations), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.67(a) (Equipment cleaning and maintenance), 1 time.
Has Revlon, Inc. received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Revlon, Inc.; the most recent is dated Jun 2, 2026.