Kenlor Industries, Inc.
FDA inspection history in Santa Ana, California, 2019 to 2020
- 2
- Form 483s
Every document, by year
- Form 483
2019: one Form 483; 2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019–20Two Form 483s, at Santa Ana, California.
- 2020The longest 483 on file: 5 observations over 5 pages at Santa Ana, California.
Cited most
Across all Kenlor Industries observations on file
- 21 CFR 820.181Device master record1
- 21 CFR 820.184Device history record1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.25(b)Personnel1
- 21 CFR 820.30(a)Design controls1
The complete Kenlor Industries 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
Santa Ana, California
Two Form 483s · 2019 to 2020 · 8 observations
Latest: Form 483, Sep 21, 2020 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-09-21 | 483 Form 483 | Santa Ana, California | 5 | $99 |
| 2019-05-03 | 483 Form 483 | Santa Ana, California | 3 | $99 |
Investigators on these documents
FEI number 2027370 · most recent document Sep 21, 2020
About Kenlor Industries, Inc.
How many FDA Form 483s has Kenlor Industries, Inc. received?
FDA Intel has 2 Form 483s on file for Kenlor Industries, Inc.; the most recent is dated Sep 21, 2020.
When was Kenlor Industries, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Kenlor Industries, Inc. is a Form 483 dated Sep 21, 2020, for the site in Santa Ana, California.
What did FDA cite at Kenlor Industries, Inc.?
The regulations cited most in the observations on file for Kenlor Industries, Inc. are 21 CFR 820.181 (Device master record), 1 time; 21 CFR 820.184 (Device history record), 1 time; 21 CFR 820.22 (Quality audit), 1 time.