Person and Covey
FDA inspection history in Glendale, California, 2020 to 2025
- 2
- Form 483s
- 1
- Warning letter
Every document, by year
- Warning letter
- Form 483
2020: one Form 483; 2025: one warning letter and one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Glendale, California.
- 2025One warning letter and one Form 483, at Glendale, California.
- 2025The longest 483 on file: 7 observations over 6 pages at Glendale, California.
Cited most
Across all Person and Covey observations on file
- 21 CFR 211.100(a)Written procedures; deviations2
- 21 CFR 211.166(a)(2)Stability testing2
- 21 CFR 211.180(b)General requirements2
- 21 CFR 211.113(a)Control of microbiological contamination1
- 21 CFR 211.160(b)General requirements1
The complete Person and Covey 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
Glendale, California
Two Form 483s and one warning letter · 2020 to 2025 · 13 observations
Latest: Warning letter, Sep 23, 2025 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-09-23 | Warning letter Warning letter | Glendale, California | — | $99 |
| 2025-02-06 | 483 Form 483 | Glendale, California | 7 | $99 |
| 2020-01-30 | 483 Form 483 | Glendale, California | 6 | $99 |
Investigators on these documents
FEI number 2011222 · most recent document Sep 23, 2025
About Person and Covey
How many FDA Form 483s has Person and Covey received?
FDA Intel has 2 Form 483s on file for Person and Covey; the most recent is dated Feb 6, 2025.
When was Person and Covey last inspected by FDA?
The most recent FDA inspection document on file for Person and Covey is a Form 483 dated Feb 6, 2025, for the site in Glendale, California.
What did FDA cite at Person and Covey?
The regulations cited most in the observations on file for Person and Covey are 21 CFR 211.100(a) (Written procedures; deviations), 2 times; 21 CFR 211.166(a)(2) (Stability testing), 2 times; 21 CFR 211.180(b) (General requirements), 2 times.
Has Person and Covey received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Person and Covey; the most recent is dated Sep 23, 2025.