Daizo Corporation
FDA inspection history in Kyoto, 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 Kyoto, Japan.
Cited most
Across all Daizo observations on file
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.194(a)(4)Laboratory records1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete Daizo file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Kyoto, Japan
One Form 483 · 2023 · 3 observations
Latest: Form 483, Nov 6, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-11-06 | 483 Form 483 | Kyoto, Japan | 3 | $99 |
Investigators on these documents
FEI number 3008470621 · most recent document Nov 6, 2023
About Daizo Corporation
How many FDA Form 483s has Daizo Corporation received?
FDA Intel has 1 Form 483 on file for Daizo Corporation; the most recent is dated Nov 6, 2023.
When was Daizo Corporation last inspected by FDA?
The most recent FDA inspection document on file for Daizo Corporation is a Form 483 dated Nov 6, 2023, for the site in Kyoto, Japan.
What did FDA cite at Daizo Corporation?
The regulations cited most in the observations on file for Daizo Corporation are 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.194(a)(4) (Laboratory records), 1 time; 21 CFR 211.68(b) (Automatic, mechanical, and electronic equipment), 1 time.