Ningxia Qiyuan Pharmaceutical Co., Ltd.
FDA inspection history in Yinchuan, 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 Yinchuan, China.
Cited most
Across all Ningxia Qiyuan Pharmaceutical Co. observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.160General requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.28Personnel responsibilities1
- 21 CFR 211.58Maintenance1
The complete Ningxia Qiyuan Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Yinchuan, China
One Form 483 · 2019 · 6 observations
Latest: Form 483, Jun 28, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-06-28 | 483 Form 483 | Yinchuan, China | 6 | $99 |
Investigators on these documents
FEI number 3004341367 · most recent document Jun 28, 2019
About Ningxia Qiyuan Pharmaceutical Co., Ltd.
How many FDA Form 483s has Ningxia Qiyuan Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Ningxia Qiyuan Pharmaceutical Co., Ltd.; the most recent is dated Jun 28, 2019.
When was Ningxia Qiyuan Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Ningxia Qiyuan Pharmaceutical Co., Ltd. is a Form 483 dated Jun 28, 2019, for the site in Yinchuan, China.
What did FDA cite at Ningxia Qiyuan Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Ningxia Qiyuan Pharmaceutical Co., Ltd. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.