Hangzhou Huadong Medicine Group Kangrun Pharmaceutical
FDA inspection history in Xiaofeng Town, Anji, China, 2015
- 1
- Form 483
Every document, by year
- Form 483
2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Xiaofeng Town, Anji, China.
Cited most
Across all Hangzhou Huadong Medicine Group Kangrun Pharmaceutical observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.166Stability testing1
The complete Hangzhou Huadong Medicine Group Kangrun Pharmaceutical file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Xiaofeng Town, Anji, China
One Form 483 · 2015 · 7 observations
Latest: Form 483, Jan 22, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-01-22 | 483 Form 483 | Xiaofeng Town, Anji, China | 7 | $99 |
Investigators on these documents
FEI number 3008465758 · most recent document Jan 22, 2015
About Hangzhou Huadong Medicine Group Kangrun Pharmaceutical
How many FDA Form 483s has Hangzhou Huadong Medicine Group Kangrun Pharmaceutical received?
FDA Intel has 1 Form 483 on file for Hangzhou Huadong Medicine Group Kangrun Pharmaceutical; the most recent is dated Jan 22, 2015.
When was Hangzhou Huadong Medicine Group Kangrun Pharmaceutical last inspected by FDA?
The most recent FDA inspection document on file for Hangzhou Huadong Medicine Group Kangrun Pharmaceutical is a Form 483 dated Jan 22, 2015, for the site in Xiaofeng Town, Anji, China.
What did FDA cite at Hangzhou Huadong Medicine Group Kangrun Pharmaceutical?
The regulations cited most in the observations on file for Hangzhou Huadong Medicine Group Kangrun Pharmaceutical are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time.