FEI 3018521591
FDA inspection history in Glendale, California, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Glendale, California.
Cited most
Across all site observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.67(b)Equipment cleaning and maintenance1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
- 21 CFR 211.84(d)(2)Testing and approval or rejection of components, drug product containers, and closures1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Glendale, California
One Form 483 · 2025 · 4 observations
Latest: Form 483, Mar 18, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-03-18 | 483 Form 483 | Glendale, California | 4 | $99 |
Investigators on these documents
FEI number 3018521591 · most recent document Mar 18, 2025
About FEI 3018521591
How many FDA Form 483s has FEI 3018521591 received?
FDA Intel has 1 Form 483 on file for FEI 3018521591; the most recent is dated Mar 18, 2025.
When was FEI 3018521591 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3018521591 is a Form 483 dated Mar 18, 2025, for the site in Glendale, California.
What did FDA cite at FEI 3018521591?
The regulations cited most in the observations on file for FEI 3018521591 are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.67(b) (Equipment cleaning and maintenance), 1 time; 21 CFR 211.68(b) (Automatic, mechanical, and electronic equipment), 1 time.