Hisun Pfizer Pharmaceuticals Co., Ltd
FDA inspection history in Fuyang, China, 2015
- 1
- Form 483
Every document, by year
- Form 483
2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Fuyang, China.
Cited most
Across all Hisun Pfizer Pharmaceuticals Co. observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.194Laboratory records2
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.25Personnel qualifications1
- 21 CFR 211.42Design and construction features1
The complete Hisun Pfizer Pharmaceuticals Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Fuyang, China
One Form 483 · 2015 · 6 observations
Latest: Form 483, Apr 24, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-04-24 | 483 Form 483 | Fuyang, China | 6 | $99 |
Investigators on these documents
FEI number 3010820594 · most recent document Apr 24, 2015
About Hisun Pfizer Pharmaceuticals Co., Ltd
How many FDA Form 483s has Hisun Pfizer Pharmaceuticals Co., Ltd received?
FDA Intel has 1 Form 483 on file for Hisun Pfizer Pharmaceuticals Co., Ltd; the most recent is dated Apr 24, 2015.
When was Hisun Pfizer Pharmaceuticals Co., Ltd last inspected by FDA?
The most recent FDA inspection document on file for Hisun Pfizer Pharmaceuticals Co., Ltd is a Form 483 dated Apr 24, 2015, for the site in Fuyang, China.
What did FDA cite at Hisun Pfizer Pharmaceuticals Co., Ltd?
The regulations cited most in the observations on file for Hisun Pfizer Pharmaceuticals Co., Ltd are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.194 (Laboratory records), 2 times; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times.