Hubei HONCH Pharmaceutical Co., Ltd.
FDA inspection history in Huanggang, 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 Huanggang, China.
Cited most
Across all Hubei HONCH Pharmaceutical Co. observations on file
- 21 CFR 211.42Design and construction features1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Hubei HONCH Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Huanggang, China
One Form 483 · 2019
Latest: Form 483, Mar 22, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-03-22 | 483 Form 483 | Huanggang, China | — | $99 |
FEI number 3009478588 · most recent document Mar 22, 2019
About Hubei HONCH Pharmaceutical Co., Ltd.
How many FDA Form 483s has Hubei HONCH Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Hubei HONCH Pharmaceutical Co., Ltd.; the most recent is dated Mar 22, 2019.
When was Hubei HONCH Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Hubei HONCH Pharmaceutical Co., Ltd. is a Form 483 dated Mar 22, 2019, for the site in Huanggang, China.
What did FDA cite at Hubei HONCH Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Hubei HONCH Pharmaceutical Co., Ltd. are 21 CFR 211.42 (Design and construction features), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.