Genus Lifesciences Inc.
FDA inspection history in Allentown, Pennsylvania, 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 Allentown, Pennsylvania.
Cited most
Across all Genus Lifesciences observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.192Production record review1
- 21 CFR 314.81(b)(1)(ii)Other postmarketing reports1
The complete Genus Lifesciences file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Allentown, Pennsylvania
One Form 483 · 2019 · 3 observations
Latest: Form 483, Sep 20, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-09-20 | 483 Form 483 | Allentown, Pennsylvania | 3 | $99 |
Investigators on these documents
FEI number 3003851100 · most recent document Sep 20, 2019
About Genus Lifesciences Inc.
How many FDA Form 483s has Genus Lifesciences Inc. received?
FDA Intel has 1 Form 483 on file for Genus Lifesciences Inc.; the most recent is dated Sep 20, 2019.
When was Genus Lifesciences Inc. last inspected by FDA?
The most recent FDA inspection document on file for Genus Lifesciences Inc. is a Form 483 dated Sep 20, 2019, for the site in Allentown, Pennsylvania.
What did FDA cite at Genus Lifesciences Inc.?
The regulations cited most in the observations on file for Genus Lifesciences Inc. are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 314.81(b)(1)(ii) (Other postmarketing reports), 1 time.