KDL Precision Molding
FDA inspection history in Pacoima, California, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Pacoima, California.
Cited most
Across all KDL Precision Molding observations on file
- 21 CFR 820.120Device labeling1
- 21 CFR 820.75(c)Process validation1
The complete KDL Precision Molding file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Pacoima, California
One Form 483 · 2019 · 2 observations
Latest: Form 483, Feb 7, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-02-07 | 483 Form 483 | Pacoima, California | 2 | $99 |
Investigators on these documents
FEI number 3002941807 · most recent document Feb 7, 2019
About KDL Precision Molding
How many FDA Form 483s has KDL Precision Molding received?
FDA Intel has 1 Form 483 on file for KDL Precision Molding; the most recent is dated Feb 7, 2019.
When was KDL Precision Molding last inspected by FDA?
The most recent FDA inspection document on file for KDL Precision Molding is a Form 483 dated Feb 7, 2019, for the site in Pacoima, California.
What did FDA cite at KDL Precision Molding?
The regulations cited most in the observations on file for KDL Precision Molding are 21 CFR 820.120 (Device labeling), 1 time; 21 CFR 820.75(c) (Process validation), 1 time.