Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (API site)
FDA inspection history in Lianyungang, 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 Lianyungang, China.
Cited most
Across all Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (API site) observations on file
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (API site) file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Lianyungang, China
One Form 483 · 2015 · 2 observations
Latest: Form 483, Apr 22, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-04-22 | 483 Form 483 | Lianyungang, China | 2 | $99 |
Investigators on these documents
FEI number 3007086869 · most recent document Apr 22, 2015
About Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (API site)
How many FDA Form 483s has Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (API site) received?
FDA Intel has 1 Form 483 on file for Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (API site); the most recent is dated Apr 22, 2015.
When was Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (API site) last inspected by FDA?
The most recent FDA inspection document on file for Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (API site) is a Form 483 dated Apr 22, 2015, for the site in Lianyungang, China.
What did FDA cite at Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (API site)?
The regulations cited most in the observations on file for Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (API site) are 21 CFR 211.186 (Master production and control records), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.