Zhejiang Dingtai Pharmaceutical Co., Ltd
FDA inspection history in Tongxiang, 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 Tongxiang, China.
Cited most
Across all Zhejiang Dingtai Pharmaceutical Co. observations on file
- 21 CFR 211.188Batch production and control records3
- 21 CFR 211.160General requirements1
- 21 CFR 211.194Laboratory records1
The complete Zhejiang Dingtai Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Tongxiang, China
One Form 483 · 2019 · 4 observations
Latest: Form 483, Jan 25, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-01-25 | 483 Form 483 | Tongxiang, China | 4 | $99 |
Investigators on these documents
FEI number 3011302639 · most recent document Jan 25, 2019
About Zhejiang Dingtai Pharmaceutical Co., Ltd
How many FDA Form 483s has Zhejiang Dingtai Pharmaceutical Co., Ltd received?
FDA Intel has 1 Form 483 on file for Zhejiang Dingtai Pharmaceutical Co., Ltd; the most recent is dated Jan 25, 2019.
When was Zhejiang Dingtai Pharmaceutical Co., Ltd last inspected by FDA?
The most recent FDA inspection document on file for Zhejiang Dingtai Pharmaceutical Co., Ltd is a Form 483 dated Jan 25, 2019, for the site in Tongxiang, China.
What did FDA cite at Zhejiang Dingtai Pharmaceutical Co., Ltd?
The regulations cited most in the observations on file for Zhejiang Dingtai Pharmaceutical Co., Ltd are 21 CFR 211.188 (Batch production and control records), 3 times; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.194 (Laboratory records), 1 time.