Zhejiang Cheng Yi Pharmaceutical Co., Ltd.
FDA inspection history in Wenzhou City, 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 Wenzhou City, China.
Cited most
Across all Zhejiang Cheng Yi Pharmaceutical Co. observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.142(b)Warehousing procedures1
- 21 CFR 211.22(a)Responsibilities of quality control unit1
The complete Zhejiang Cheng Yi Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Wenzhou City, China
One Form 483 · 2019 · 4 observations
Latest: Form 483, Nov 22, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-11-22 | 483 Form 483 | Wenzhou City, China | 4 | $99 |
Investigators on these documents
FEI number 3004090742 · most recent document Nov 22, 2019
About Zhejiang Cheng Yi Pharmaceutical Co., Ltd.
How many FDA Form 483s has Zhejiang Cheng Yi Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Zhejiang Cheng Yi Pharmaceutical Co., Ltd.; the most recent is dated Nov 22, 2019.
When was Zhejiang Cheng Yi Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Zhejiang Cheng Yi Pharmaceutical Co., Ltd. is a Form 483 dated Nov 22, 2019, for the site in Wenzhou City, China.
What did FDA cite at Zhejiang Cheng Yi Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Zhejiang Cheng Yi Pharmaceutical Co., Ltd. are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.142(b) (Warehousing procedures), 1 time.