Yichang Sanxia Pharmaceutical Co., Ltd.
FDA inspection history in Yichang, China, 2016
- 1
- Form 483
Every document, by year
- Form 483
2016: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Yichang, China.
Cited most
Across all Yichang Sanxia Pharmaceutical Co. observations on file
- 21 CFR 211.166Stability testing1
- 21 CFR 211.194Laboratory records1
The complete Yichang Sanxia Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Yichang, China
One Form 483 · 2016 · 2 observations
Latest: Form 483, Jul 15, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-07-15 | 483 Form 483 | Yichang, China | 2 | $99 |
Investigators on these documents
FEI number 3003274512 · most recent document Jul 15, 2016
About Yichang Sanxia Pharmaceutical Co., Ltd.
How many FDA Form 483s has Yichang Sanxia Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Yichang Sanxia Pharmaceutical Co., Ltd.; the most recent is dated Jul 15, 2016.
When was Yichang Sanxia Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Yichang Sanxia Pharmaceutical Co., Ltd. is a Form 483 dated Jul 15, 2016, for the site in Yichang, China.
What did FDA cite at Yichang Sanxia Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Yichang Sanxia Pharmaceutical Co., Ltd. are 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.194 (Laboratory records), 1 time.