Qilu Pharmaceutical Co., Ltd.
FDA inspection history in Jinan, 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 Jinan, China.
Cited most
Across all Qilu Pharmaceutical Co. observations on file
- 21 CFR 211.142Warehousing procedures1
- 21 CFR 211.192Production record review1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Qilu Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Jinan, China
One Form 483 · 2018 · 2 observations
Latest: Form 483, Feb 22, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-02-22 | 483 Form 483 | Jinan, China | 2 | $99 |
Investigators on these documents
FEI number 3003674637 · most recent document Feb 22, 2018
About Qilu Pharmaceutical Co., Ltd.
How many FDA Form 483s has Qilu Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Qilu Pharmaceutical Co., Ltd.; the most recent is dated Feb 22, 2018.
When was Qilu Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Qilu Pharmaceutical Co., Ltd. is a Form 483 dated Feb 22, 2018, for the site in Jinan, China.
What did FDA cite at Qilu Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Qilu Pharmaceutical Co., Ltd. are 21 CFR 211.142 (Warehousing procedures), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.