Vortech Pharmaceuticals, Ltd.
FDA inspection history in Dearborn, Michigan, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Dearborn, Michigan.
Cited most
Across all Vortech Pharmaceuticals observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.165(b)Testing and release for distribution1
- 21 CFR 211.180(e)(2)General requirements1
The complete Vortech Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Dearborn, Michigan
One Form 483 · 2022 · 4 observations
Latest: Form 483, Feb 9, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-02-09 | 483 Form 483 | Dearborn, Michigan | 4 | $99 |
FEI number 1810390 · most recent document Feb 9, 2022
About Vortech Pharmaceuticals, Ltd.
How many FDA Form 483s has Vortech Pharmaceuticals, Ltd. received?
FDA Intel has 1 Form 483 on file for Vortech Pharmaceuticals, Ltd.; the most recent is dated Feb 9, 2022.
When was Vortech Pharmaceuticals, Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Vortech Pharmaceuticals, Ltd. is a Form 483 dated Feb 9, 2022, for the site in Dearborn, Michigan.
What did FDA cite at Vortech Pharmaceuticals, Ltd.?
The regulations cited most in the observations on file for Vortech Pharmaceuticals, Ltd. are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.165(b) (Testing and release for distribution), 1 time.