Zhejiang Jingwei Pharmaceutical Co., Ltd.
FDA inspection history in Quzhou, 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 Quzhou, China.
Cited most
Across all Zhejiang Jingwei Pharmaceutical Co. observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.142Warehousing procedures1
- 21 CFR 211.160General requirements1
- 21 CFR 211.198Complaint files1
- 21 CFR 211.58Maintenance1
The complete Zhejiang Jingwei Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Quzhou, China
One Form 483 · 2019 · 6 observations
Latest: Form 483, Mar 15, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-03-15 | 483 Form 483 | Quzhou, China | 6 | $99 |
Investigators on these documents
FEI number 3010166839 · most recent document Mar 15, 2019
About Zhejiang Jingwei Pharmaceutical Co., Ltd.
How many FDA Form 483s has Zhejiang Jingwei Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Zhejiang Jingwei Pharmaceutical Co., Ltd.; the most recent is dated Mar 15, 2019.
When was Zhejiang Jingwei Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Zhejiang Jingwei Pharmaceutical Co., Ltd. is a Form 483 dated Mar 15, 2019, for the site in Quzhou, China.
What did FDA cite at Zhejiang Jingwei Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Zhejiang Jingwei Pharmaceutical Co., Ltd. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.142 (Warehousing procedures), 1 time; 21 CFR 211.160 (General requirements), 1 time.