Zhejiang Charioteer 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 Charioteer Pharmaceutical Co. observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.192Production record review1
- 21 CFR 211.198Complaint files1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Zhejiang Charioteer Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Taizhou, China
One Form 483 · 2018 · 2 observations
Latest: Form 483, Jan 18, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-01-18 | 483 Form 483 | Taizhou, China | 2 | $99 |
Investigators on these documents
FEI number 3002808516 · most recent document Jan 18, 2018
About Zhejiang Charioteer Pharmaceutical Co., Ltd.
How many FDA Form 483s has Zhejiang Charioteer Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Zhejiang Charioteer Pharmaceutical Co., Ltd.; the most recent is dated Jan 18, 2018.
When was Zhejiang Charioteer Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Zhejiang Charioteer Pharmaceutical Co., Ltd. is a Form 483 dated Jan 18, 2018, for the site in Taizhou, China.
What did FDA cite at Zhejiang Charioteer Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Zhejiang Charioteer Pharmaceutical Co., Ltd. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.198 (Complaint files), 1 time.