FEI 3042366712
FDA inspection history in Phoenix, Arizona, 2026
- 1
- Form 483
Every document, by year
- Form 483
2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2026One Form 483, at Phoenix, Arizona.
Cited most
Across all site observations on file
- 21 CFR 312.60General responsibilities of investigators1
- 21 CFR 312.62(b)Investigator recordkeeping and record retention1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Phoenix, Arizona
One Form 483 · 2026 · 2 observations
Latest: Form 483, Mar 13, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-03-13 | 483 Form 483 | Phoenix, Arizona | 2 | $99 |
Investigators on these documents
FEI number 3042366712 · most recent document Mar 13, 2026
About FEI 3042366712
How many FDA Form 483s has FEI 3042366712 received?
FDA Intel has 1 Form 483 on file for FEI 3042366712; the most recent is dated Mar 13, 2026.
When was FEI 3042366712 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3042366712 is a Form 483 dated Mar 13, 2026, for the site in Phoenix, Arizona.
What did FDA cite at FEI 3042366712?
The regulations cited most in the observations on file for FEI 3042366712 are 21 CFR 312.60 (General responsibilities of investigators), 1 time; 21 CFR 312.62(b) (Investigator recordkeeping and record retention), 1 time.