Yancheng Suhai Pharmaceutical Co. Ltd.
FDA inspection history in Yancheng, 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 Yancheng, China.
Cited most
Across all Yancheng Suhai Pharmaceutical Co. observations on file
- 21 CFR 211.67Equipment cleaning and maintenance3
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.25Personnel qualifications1
- 21 CFR 211.42Design and construction features1
The complete Yancheng Suhai Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Yancheng, China
One Form 483 · 2019 · 7 observations
Latest: Form 483, Apr 26, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-04-26 | 483 Form 483 | Yancheng, China | 7 | $99 |
FEI number 3002394098 · most recent document Apr 26, 2019
About Yancheng Suhai Pharmaceutical Co. Ltd.
How many FDA Form 483s has Yancheng Suhai Pharmaceutical Co. Ltd. received?
FDA Intel has 1 Form 483 on file for Yancheng Suhai Pharmaceutical Co. Ltd.; the most recent is dated Apr 26, 2019.
When was Yancheng Suhai Pharmaceutical Co. Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Yancheng Suhai Pharmaceutical Co. Ltd. is a Form 483 dated Apr 26, 2019, for the site in Yancheng, China.
What did FDA cite at Yancheng Suhai Pharmaceutical Co. Ltd.?
The regulations cited most in the observations on file for Yancheng Suhai Pharmaceutical Co. Ltd. are 21 CFR 211.67 (Equipment cleaning and maintenance), 3 times; 21 CFR 211.188 (Batch production and control records), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.