Laboratoires KABS Inc
FDA inspection history in Val-des-Sources, Canada, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Val-des-Sources, Canada.
Cited most
Across all Laboratoires KABS observations on file
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 820.100Corrective and preventive action1
- 21 CFR 820.75Process validation1
The complete Laboratoires KABS file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Val-des-Sources, Canada
One Form 483 · 2024 · 3 observations
Latest: Form 483, Jan 25, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-01-25 | 483 Form 483 | Val-des-Sources, Canada | 3 | $99 |
Investigators on these documents
FEI number 3019551074 · most recent document Jan 25, 2024
About Laboratoires KABS Inc
How many FDA Form 483s has Laboratoires KABS Inc received?
FDA Intel has 1 Form 483 on file for Laboratoires KABS Inc; the most recent is dated Jan 25, 2024.
When was Laboratoires KABS Inc last inspected by FDA?
The most recent FDA inspection document on file for Laboratoires KABS Inc is a Form 483 dated Jan 25, 2024, for the site in Val-des-Sources, Canada.
What did FDA cite at Laboratoires KABS Inc?
The regulations cited most in the observations on file for Laboratoires KABS Inc are 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 820.100 (Corrective and preventive action), 1 time; 21 CFR 820.75 (Process validation), 1 time.