Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API)
FDA inspection history in Xianju, China, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Xianju, China.
Cited most
Across all Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API) observations on file
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API) file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Xianju, China
One Form 483 · 2019 · 1 observation
Latest: Form 483, Aug 23, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-08-23 | 483 Form 483 | Xianju, China | 1 | $99 |
Investigators on these documents
FEI number 3003663256 · most recent document Aug 23, 2019
About Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API)
How many FDA Form 483s has Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API) received?
FDA Intel has 1 Form 483 on file for Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API); the most recent is dated Aug 23, 2019.
When was Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API) last inspected by FDA?
The most recent FDA inspection document on file for Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API) is a Form 483 dated Aug 23, 2019, for the site in Xianju, China.
What did FDA cite at Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API)?
The regulations cited most in the observations on file for Zhejiang Xianju Pharmaceutical Co., Ltd. (Yangfu API) are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.