Taiho Pharmaceutical Co., Ltd.
FDA inspection history in Takabo, Japan, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Takabo, Japan.
Cited most
Across all Taiho Pharmaceutical Co. observations on file
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.68(a)Automatic, mechanical, and electronic equipment1
The complete Taiho Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Takabo, Japan
One Form 483 · 2024 · 2 observations
Latest: Form 483, Jan 26, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-01-26 | 483 Form 483 | Takabo, Japan | 2 | $99 |
FEI number 3010872322 · most recent document Jan 26, 2024
About Taiho Pharmaceutical Co., Ltd.
How many FDA Form 483s has Taiho Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Taiho Pharmaceutical Co., Ltd.; the most recent is dated Jan 26, 2024.
When was Taiho Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Taiho Pharmaceutical Co., Ltd. is a Form 483 dated Jan 26, 2024, for the site in Takabo, Japan.
What did FDA cite at Taiho Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Taiho Pharmaceutical Co., Ltd. are 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.68(a) (Automatic, mechanical, and electronic equipment), 1 time.