Retivue Lie
FDA inspection history in Charlottesville, Virginia, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Charlottesville, Virginia.
Cited most
Across all Retivue Lie observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.20(c)Management responsibility1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.50(a)(1)Purchasing controls1
- 21 CFR 820.80(a)Receiving, in-process, and finished device acceptance1
The complete Retivue Lie file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Charlottesville, Virginia
One Form 483 · 2024 · 5 observations
Latest: Form 483, Apr 17, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-04-17 | 483 Form 483 | Charlottesville, Virginia | 5 | $99 |
Investigators on these documents
FEI number 3019541696 · most recent document Apr 17, 2024
About Retivue Lie
How many FDA Form 483s has Retivue Lie received?
FDA Intel has 1 Form 483 on file for Retivue Lie; the most recent is dated Apr 17, 2024.
When was Retivue Lie last inspected by FDA?
The most recent FDA inspection document on file for Retivue Lie is a Form 483 dated Apr 17, 2024, for the site in Charlottesville, Virginia.
What did FDA cite at Retivue Lie?
The regulations cited most in the observations on file for Retivue Lie are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.20(c) (Management responsibility), 1 time; 21 CFR 820.22 (Quality audit), 1 time.