Zhejiang Huazhou Pharmaceutical Co., Ltd.
FDA inspection history in Taizhou, China, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Taizhou, China.
Cited most
Across all Zhejiang Huazhou Pharmaceutical Co. observations on file
- 21 CFR 211.194Laboratory records2
- 21 CFR 211.182Equipment cleaning and use log1
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.192Production record review1
- 21 CFR 211.56Sanitation1
The complete Zhejiang Huazhou Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Taizhou, China
One Form 483 · 2018 · 8 observations
Latest: Form 483, Mar 22, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-03-22 | 483 Form 483 | Taizhou, China | 8 | $99 |
Investigators on these documents
FEI number 3012672996 · most recent document Mar 22, 2018
About Zhejiang Huazhou Pharmaceutical Co., Ltd.
How many FDA Form 483s has Zhejiang Huazhou Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Zhejiang Huazhou Pharmaceutical Co., Ltd.; the most recent is dated Mar 22, 2018.
When was Zhejiang Huazhou Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Zhejiang Huazhou Pharmaceutical Co., Ltd. is a Form 483 dated Mar 22, 2018, for the site in Taizhou, China.
What did FDA cite at Zhejiang Huazhou Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Zhejiang Huazhou Pharmaceutical Co., Ltd. are 21 CFR 211.194 (Laboratory records), 2 times; 21 CFR 211.182 (Equipment cleaning and use log), 1 time; 21 CFR 211.186 (Master production and control records), 1 time.