Sichuan Qingmu Pharmaceutical Co., Ltd.
FDA inspection history in Meishan, China, 2021
- 1
- Form 483
Every document, by year
- Form 483
2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One Form 483, at Meishan, China.
Cited most
Across all Sichuan Qingmu Pharmaceutical Co. observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Sichuan Qingmu Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Meishan, China
One Form 483 · 2021
Latest: Form 483, Sep 7, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-09-07 | 483 Form 483 | Meishan, China | — | $99 |
Investigators on these documents
FEI number 3014747858 · most recent document Sep 7, 2021
About Sichuan Qingmu Pharmaceutical Co., Ltd.
How many FDA Form 483s has Sichuan Qingmu Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Sichuan Qingmu Pharmaceutical Co., Ltd.; the most recent is dated Sep 7, 2021.
When was Sichuan Qingmu Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Sichuan Qingmu Pharmaceutical Co., Ltd. is a Form 483 dated Sep 7, 2021, for the site in Meishan, China.
What did FDA cite at Sichuan Qingmu Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Sichuan Qingmu Pharmaceutical Co., Ltd. are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.