Vernon Packaging, Inc
FDA inspection history in Mount Vernon, New York, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Mount Vernon, New York.
Cited most
Across all Vernon Packaging observations on file
- 21 CFR 211.22(a)Responsibilities of quality control unit2
- 21 CFR 211.101(c)(3)Charge-in of components1
The complete Vernon Packaging file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Mount Vernon, New York
One Form 483 · 2017 · 3 observations
Latest: Form 483, Nov 8, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-11-08 | 483 Form 483 | Mount Vernon, New York | 3 | $99 |
Investigators on these documents
FEI number 3003561815 · most recent document Nov 8, 2017
About Vernon Packaging, Inc
How many FDA Form 483s has Vernon Packaging, Inc received?
FDA Intel has 1 Form 483 on file for Vernon Packaging, Inc; the most recent is dated Nov 8, 2017.
When was Vernon Packaging, Inc last inspected by FDA?
The most recent FDA inspection document on file for Vernon Packaging, Inc is a Form 483 dated Nov 8, 2017, for the site in Mount Vernon, New York.
What did FDA cite at Vernon Packaging, Inc?
The regulations cited most in the observations on file for Vernon Packaging, Inc are 21 CFR 211.22(a) (Responsibilities of quality control unit), 2 times; 21 CFR 211.101(c)(3) (Charge-in of components), 1 time.