Icrco, Inc
FDA inspection history in Goleta, California, 2016
- 1
- Form 483
Every document, by year
- Form 483
2016: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Goleta, California.
Cited most
Across all Icrco observations on file
- 21 CFR 820.120Device labeling1
- 21 CFR 820.184Device history record1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.70(a)Production and process controls1
The complete Icrco file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Goleta, California
One Form 483 · 2016 · 4 observations
Latest: Form 483, Sep 15, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-09-15 | 483 Form 483 | Goleta, California | 4 | $99 |
Investigators on these documents
FEI number 3009717300 · most recent document Sep 15, 2016
About Icrco, Inc
How many FDA Form 483s has Icrco, Inc received?
FDA Intel has 1 Form 483 on file for Icrco, Inc; the most recent is dated Sep 15, 2016.
When was Icrco, Inc last inspected by FDA?
The most recent FDA inspection document on file for Icrco, Inc is a Form 483 dated Sep 15, 2016, for the site in Goleta, California.
What did FDA cite at Icrco, Inc?
The regulations cited most in the observations on file for Icrco, Inc are 21 CFR 820.120 (Device labeling), 1 time; 21 CFR 820.184 (Device history record), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time.