Yabao Pharmaceutical Co., Ltd.
FDA inspection history in Beijing, China, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Beijing, China.
Cited most
Across all Yabao Pharmaceutical Co. observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.192Production record review1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Yabao Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Beijing, China
One Form 483 · 2022
Latest: Form 483, Apr 20, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-04-20 | 483 Form 483 | Beijing, China | — | $99 |
FEI number 3009071264 · most recent document Apr 20, 2022
About Yabao Pharmaceutical Co., Ltd.
How many FDA Form 483s has Yabao Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Yabao Pharmaceutical Co., Ltd.; the most recent is dated Apr 20, 2022.
When was Yabao Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Yabao Pharmaceutical Co., Ltd. is a Form 483 dated Apr 20, 2022, for the site in Beijing, China.
What did FDA cite at Yabao Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Yabao Pharmaceutical Co., Ltd. are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.