FEI 3004010435
FDA inspection history in Salt Lake City, Utah, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Salt Lake City, Utah.
Cited most
Across all site observations on file
- 21 CFR 211.180General requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Salt Lake City, Utah
One Form 483 · 2024 · 1 observation
Latest: Form 483, Sep 6, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-09-06 | 483 Form 483 | Salt Lake City, Utah | 1 | $99 |
Investigators on these documents
FEI number 3004010435 · most recent document Sep 6, 2024
About FEI 3004010435
How many FDA Form 483s has FEI 3004010435 received?
FDA Intel has 1 Form 483 on file for FEI 3004010435; the most recent is dated Sep 6, 2024.
When was FEI 3004010435 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3004010435 is a Form 483 dated Sep 6, 2024, for the site in Salt Lake City, Utah.
What did FDA cite at FEI 3004010435?
The regulations cited most in the observations on file for FEI 3004010435 are 21 CFR 211.180 (General requirements), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.