Intergel Pharmaceutical Inc
FDA inspection history in Irvington, New Jersey, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Irvington, New Jersey.
Cited most
Across all Intergel Pharmaceutical observations on file
- 21 CFR 211.180General requirements1
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Intergel Pharmaceutical file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Irvington, New Jersey
One Form 483 · 2018 · 2 observations
Latest: Form 483, Nov 20, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-11-20 | 483 Form 483 | Irvington, New Jersey | 2 | $99 |
FEI number 1000526797 · most recent document Nov 20, 2018
About Intergel Pharmaceutical Inc
How many FDA Form 483s has Intergel Pharmaceutical Inc received?
FDA Intel has 1 Form 483 on file for Intergel Pharmaceutical Inc; the most recent is dated Nov 20, 2018.
When was Intergel Pharmaceutical Inc last inspected by FDA?
The most recent FDA inspection document on file for Intergel Pharmaceutical Inc is a Form 483 dated Nov 20, 2018, for the site in Irvington, New Jersey.
What did FDA cite at Intergel Pharmaceutical Inc?
The regulations cited most in the observations on file for Intergel Pharmaceutical Inc are 21 CFR 211.180 (General requirements), 1 time; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.