AGC Inc.
FDA inspection history in Ichihara, Japan, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Ichihara, Japan.
Cited most
Across all AGC observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.122Materials examination and usage criteria1
- 21 CFR 211.125Labeling issuance1
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
The complete AGC file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Ichihara, Japan
One Form 483 · 2023 · 3 observations
Latest: Form 483, Oct 27, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-10-27 | 483 Form 483 | Ichihara, Japan | 3 | $99 |
FEI number 3003282601 · most recent document Oct 27, 2023
About AGC Inc.
How many FDA Form 483s has AGC Inc. received?
FDA Intel has 1 Form 483 on file for AGC Inc.; the most recent is dated Oct 27, 2023.
When was AGC Inc. last inspected by FDA?
The most recent FDA inspection document on file for AGC Inc. is a Form 483 dated Oct 27, 2023, for the site in Ichihara, Japan.
What did FDA cite at AGC Inc.?
The regulations cited most in the observations on file for AGC Inc. are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.122 (Materials examination and usage criteria), 1 time; 21 CFR 211.125 (Labeling issuance), 1 time.