Chifeng Pharmaceutical Co. Ltd.
FDA inspection history in Chifeng, China, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Chifeng, China.
Cited most
Across all Chifeng Pharmaceutical Co. observations on file
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.180General requirements1
- 21 CFR 211.188Batch production and control records1
The complete Chifeng Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Chifeng, China
One Form 483 · 2017 · 9 observations
Latest: Form 483, Oct 13, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-10-13 | 483 Form 483 | Chifeng, China | 9 | $99 |
Investigators on these documents
FEI number 1000390117 · most recent document Oct 13, 2017
About Chifeng Pharmaceutical Co. Ltd.
How many FDA Form 483s has Chifeng Pharmaceutical Co. Ltd. received?
FDA Intel has 1 Form 483 on file for Chifeng Pharmaceutical Co. Ltd.; the most recent is dated Oct 13, 2017.
When was Chifeng Pharmaceutical Co. Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Chifeng Pharmaceutical Co. Ltd. is a Form 483 dated Oct 13, 2017, for the site in Chifeng, China.
What did FDA cite at Chifeng Pharmaceutical Co. Ltd.?
The regulations cited most in the observations on file for Chifeng Pharmaceutical Co. Ltd. are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time.