Davion Inc
FDA inspection history in Newark, New Jersey, 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 Newark, New Jersey.
Cited most
Across all Davion observations on file
- 21 CFR 211.180General requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.46Ventilation, air filtration, air heating and cooling1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Davion file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Newark, New Jersey
One Form 483 · 2019 · 3 observations
Latest: Form 483, May 15, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-05-15 | 483 Form 483 | Newark, New Jersey | 3 | $99 |
FEI number 2245909 · most recent document May 15, 2019
About Davion Inc
How many FDA Form 483s has Davion Inc received?
FDA Intel has 1 Form 483 on file for Davion Inc; the most recent is dated May 15, 2019.
When was Davion Inc last inspected by FDA?
The most recent FDA inspection document on file for Davion Inc is a Form 483 dated May 15, 2019, for the site in Newark, New Jersey.
What did FDA cite at Davion Inc?
The regulations cited most in the observations on file for Davion Inc are 21 CFR 211.180 (General requirements), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.46 (Ventilation, air filtration, air heating and cooling), 1 time.