COSMETIC LABORATORY INC
FDA inspection history in Downey, California, 2022 to 2026
- 2
- Form 483s
Every document, by year
- Form 483
2022: one Form 483; 2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Downey, California.
- 2022The longest 483 on file: 5 observations over 6 pages at Downey, California.
- 2026One Form 483, at Downey, California.
Cited most
Across all COSMETIC LABORATORY observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.180(e)General requirements1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.67(a)Equipment cleaning and maintenance1
The complete COSMETIC LABORATORY 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
Downey, California
Two Form 483s · 2022 to 2026 · 7 observations
Latest: Form 483, Mar 10, 2026 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-03-10 | 483 Form 483 | Downey, California | 2 | $99 |
| 2022-08-03 | 483 Form 483 | Downey, California | 5 | $99 |
Investigators on these documents
Alan L. Truong (1)Darren S. Brown (1)Devisree P. Mattigiri (1)Youkeun Kim (1)
FEI number 3011959287 · most recent document Mar 10, 2026
About COSMETIC LABORATORY INC
How many FDA Form 483s has COSMETIC LABORATORY INC received?
FDA Intel has 2 Form 483s on file for COSMETIC LABORATORY INC; the most recent is dated Mar 10, 2026.
When was COSMETIC LABORATORY INC last inspected by FDA?
The most recent FDA inspection document on file for COSMETIC LABORATORY INC is a Form 483 dated Mar 10, 2026, for the site in Downey, California.
What did FDA cite at COSMETIC LABORATORY INC?
The regulations cited most in the observations on file for COSMETIC LABORATORY INC are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.180(e) (General requirements), 1 time.