Fuji Yakuhin Co., Ltd.
FDA inspection history across 2 sites, 2019 to 2022
- 2
- Form 483s
Every document, by year
- Form 483
2019: one Form 483; 2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Toyama, Japan.
- 2019The longest 483 on file: 4 observations over 3 pages at Toyama, Japan.
- 2022One Form 483, at Toyama-Shi, Japan.
Cited most
Across all Fuji Yakuhin Co. observations on file
- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.170(a)Reserve samples1
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures1
The complete Fuji Yakuhin Co. file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Toyama-Shi, Japan
One Form 483 · 2022 · 3 observations
Latest: Form 483, Nov 25, 2022 →Toyama, Japan
One Form 483 · 2019 · 4 observations
Latest: Form 483, Nov 26, 2019 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-11-25 | 483 Form 483 | Toyama-Shi, Japan | 3 | $99 |
| 2019-11-26 | 483 Form 483 | Toyama, Japan | 4 | $99 |
Investigators on these documents
FEI number 3008538640 · most recent document Nov 25, 2022
About Fuji Yakuhin Co., Ltd.
How many FDA Form 483s has Fuji Yakuhin Co., Ltd. received?
FDA Intel has 2 Form 483s on file for Fuji Yakuhin Co., Ltd.; the most recent is dated Nov 25, 2022.
When was Fuji Yakuhin Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Fuji Yakuhin Co., Ltd. is a Form 483 dated Nov 25, 2022, for the site in Toyama-Shi, Japan.
What did FDA cite at Fuji Yakuhin Co., Ltd.?
The regulations cited most in the observations on file for Fuji Yakuhin Co., Ltd. are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times; 21 CFR 211.170(a) (Reserve samples), 1 time.