Zhejiang Ruibang Laboratories
FDA inspection history in Wenzhou, China, 2016 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2016: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Wenzhou, China.
- 2024One Form 483, at Wenzhou, China.
Cited most
Across all Zhejiang Ruibang Laboratories observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.160General requirements1
- 21 CFR 211.194Laboratory records1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Zhejiang Ruibang Laboratories file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Wenzhou, China
Two Form 483s · 2016 to 2024
Latest: Form 483, Oct 25, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-10-25 | 483 Form 483 | Wenzhou, China | — | $99 |
| 2016-07-21 | 483 Form 483 | Wenzhou, China | — | $99 |
FEI number 3001027745 · most recent document Oct 25, 2024
About Zhejiang Ruibang Laboratories
How many FDA Form 483s has Zhejiang Ruibang Laboratories received?
FDA Intel has 2 Form 483s on file for Zhejiang Ruibang Laboratories; the most recent is dated Oct 25, 2024.
When was Zhejiang Ruibang Laboratories last inspected by FDA?
The most recent FDA inspection document on file for Zhejiang Ruibang Laboratories is a Form 483 dated Oct 25, 2024, for the site in Wenzhou, China.
What did FDA cite at Zhejiang Ruibang Laboratories?
The regulations cited most in the observations on file for Zhejiang Ruibang Laboratories are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.160 (General requirements), 1 time.