Kendrick Laboratories
FDA inspection history in Madison, Wisconsin, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Madison, Wisconsin.
Cited most
Across all Kendrick Laboratories observations on file
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.25(a)Personnel qualifications1
The complete Kendrick Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Madison, Wisconsin
One Form 483 · 2020 · 2 observations
Latest: Form 483, Mar 10, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-03-10 | 483 Form 483 | Madison, Wisconsin | 2 | $99 |
Investigators on these documents
FEI number 3001238747 · most recent document Mar 10, 2020
About Kendrick Laboratories
How many FDA Form 483s has Kendrick Laboratories received?
FDA Intel has 1 Form 483 on file for Kendrick Laboratories; the most recent is dated Mar 10, 2020.
When was Kendrick Laboratories last inspected by FDA?
The most recent FDA inspection document on file for Kendrick Laboratories is a Form 483 dated Mar 10, 2020, for the site in Madison, Wisconsin.
What did FDA cite at Kendrick Laboratories?
The regulations cited most in the observations on file for Kendrick Laboratories are 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.25(a) (Personnel qualifications), 1 time.