Kinbio LTD
FDA inspection history in Rehovot, Israel, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Rehovot, Israel.
Cited most
Across all Kinbio observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.192Production record review1
The complete Kinbio file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Rehovot, Israel
One Form 483 · 2022
Latest: Form 483, May 26, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-05-26 | 483 Form 483 | Rehovot, Israel | — | $99 |
FEI number 3017791608 · most recent document May 26, 2022
About Kinbio LTD
How many FDA Form 483s has Kinbio LTD received?
FDA Intel has 1 Form 483 on file for Kinbio LTD; the most recent is dated May 26, 2022.
When was Kinbio LTD last inspected by FDA?
The most recent FDA inspection document on file for Kinbio LTD is a Form 483 dated May 26, 2022, for the site in Rehovot, Israel.
What did FDA cite at Kinbio LTD?
The regulations cited most in the observations on file for Kinbio LTD are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.192 (Production record review), 1 time.