Suzhou Union Biopharm Co., Ltd.
FDA inspection history in Suzhou, China, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Suzhou, China.
Cited most
Across all Suzhou Union Biopharm Co. observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.180General requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Suzhou Union Biopharm Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Suzhou, China
One Form 483 · 2023 · 3 observations
Latest: Form 483, May 26, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-05-26 | 483 Form 483 | Suzhou, China | 3 | $99 |
Investigators on these documents
FEI number 3014164694 · most recent document May 26, 2023
About Suzhou Union Biopharm Co., Ltd.
How many FDA Form 483s has Suzhou Union Biopharm Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Suzhou Union Biopharm Co., Ltd.; the most recent is dated May 26, 2023.
When was Suzhou Union Biopharm Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Suzhou Union Biopharm Co., Ltd. is a Form 483 dated May 26, 2023, for the site in Suzhou, China.
What did FDA cite at Suzhou Union Biopharm Co., Ltd.?
The regulations cited most in the observations on file for Suzhou Union Biopharm Co., Ltd. are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.180 (General requirements), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.