FEI 3006606138
FDA inspection history in CAHERCIVEEN, Ireland, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at CAHERCIVEEN, Ireland.
Cited most
Across all site observations on file
- 21 CFR 211.160(b)(3)General requirements1
- 21 CFR 211.170(b)Reserve samples1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.68(a)Automatic, mechanical, and electronic equipment1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
CAHERCIVEEN, Ireland
One Form 483 · 2022 · 4 observations
Latest: Form 483, Jun 17, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-06-17 | 483 Form 483 | CAHERCIVEEN, Ireland | 4 | $99 |
Investigators on these documents
FEI number 3006606138 · most recent document Jun 17, 2022
About FEI 3006606138
How many FDA Form 483s has FEI 3006606138 received?
FDA Intel has 1 Form 483 on file for FEI 3006606138; the most recent is dated Jun 17, 2022.
When was FEI 3006606138 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3006606138 is a Form 483 dated Jun 17, 2022, for the site in CAHERCIVEEN, Ireland.
What did FDA cite at FEI 3006606138?
The regulations cited most in the observations on file for FEI 3006606138 are 21 CFR 211.160(b)(3) (General requirements), 1 time; 21 CFR 211.170(b) (Reserve samples), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.