BeOne Pharmaceutical (Suzhou) 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 BeOne Pharmaceutical (Suzhou) Co.,Ltd observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete BeOne Pharmaceutical (Suzhou) Co.,Ltd file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Suzhou, China
One Form 483 · 2023 · 4 observations
Latest: Form 483, Jun 16, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-06-16 | 483 Form 483 | Suzhou, China | 4 | $99 |
FEI number 3014150588 · most recent document Jun 16, 2023
About BeOne Pharmaceutical (Suzhou) Co.,Ltd
How many FDA Form 483s has BeOne Pharmaceutical (Suzhou) Co.,Ltd received?
FDA Intel has 1 Form 483 on file for BeOne Pharmaceutical (Suzhou) Co.,Ltd; the most recent is dated Jun 16, 2023.
When was BeOne Pharmaceutical (Suzhou) Co.,Ltd last inspected by FDA?
The most recent FDA inspection document on file for BeOne Pharmaceutical (Suzhou) Co.,Ltd is a Form 483 dated Jun 16, 2023, for the site in Suzhou, China.
What did FDA cite at BeOne Pharmaceutical (Suzhou) Co.,Ltd?
The regulations cited most in the observations on file for BeOne Pharmaceutical (Suzhou) Co.,Ltd are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.165 (Testing and release for distribution), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.