Oishi Koseido Co., Ltd.
FDA inspection history in Tosu, 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 Tosu, Japan.
Cited most
Across all Oishi Koseido Co. observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.122(a)Materials examination and usage criteria1
- 21 CFR 211.170(b)Reserve samples1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete Oishi Koseido Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Tosu, Japan
One Form 483 · 2023 · 6 observations
Latest: Form 483, Sep 1, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-09-01 | 483 Form 483 | Tosu, Japan | 6 | $99 |
Investigators on these documents
FEI number 3010166685 · most recent document Sep 1, 2023
About Oishi Koseido Co., Ltd.
How many FDA Form 483s has Oishi Koseido Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Oishi Koseido Co., Ltd.; the most recent is dated Sep 1, 2023.
When was Oishi Koseido Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Oishi Koseido Co., Ltd. is a Form 483 dated Sep 1, 2023, for the site in Tosu, Japan.
What did FDA cite at Oishi Koseido Co., Ltd.?
The regulations cited most in the observations on file for Oishi Koseido Co., Ltd. are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.122(a) (Materials examination and usage criteria), 1 time; 21 CFR 211.170(b) (Reserve samples), 1 time.