Devicor Medical Products Inc
FDA inspection history in Cincinnati, Ohio, 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 Cincinnati, Ohio.
Cited most
Across all Devicor Medical Products observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.30(g)Design controls1
- 21 CFR 820.40Document controls1
The complete Devicor Medical Products file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Cincinnati, Ohio
One Form 483 · 2016 · 3 observations
Latest: Form 483, Aug 1, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-08-01 | 483 Form 483 | Cincinnati, Ohio | 3 | $99 |
Investigators on these documents
FEI number 3008492462 · most recent document Aug 1, 2016
About Devicor Medical Products Inc
How many FDA Form 483s has Devicor Medical Products Inc received?
FDA Intel has 1 Form 483 on file for Devicor Medical Products Inc; the most recent is dated Aug 1, 2016.
When was Devicor Medical Products Inc last inspected by FDA?
The most recent FDA inspection document on file for Devicor Medical Products Inc is a Form 483 dated Aug 1, 2016, for the site in Cincinnati, Ohio.
What did FDA cite at Devicor Medical Products Inc?
The regulations cited most in the observations on file for Devicor Medical Products Inc are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.30(g) (Design controls), 1 time; 21 CFR 820.40 (Document controls), 1 time.