AVEM Labs LLC
FDA inspection history on file, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483.
Cited most
Across all AVEM Labs observations on file
- 21 CFR 1271.200Equipment1
- 21 CFR 1271.210Supplies and reagents1
- 21 CFR 1271.230Process validation1
- 21 CFR 1271.250Labeling controls1
- 21 CFR 1271.270Records1
The complete AVEM Labs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-05-21 | 483 Form 483 | — | 5 | $99 |
Investigators on these documents
FEI number 3017596057 · most recent document May 21, 2025
About AVEM Labs LLC
How many FDA Form 483s has AVEM Labs LLC received?
FDA Intel has 1 Form 483 on file for AVEM Labs LLC; the most recent is dated May 21, 2025.
When was AVEM Labs LLC last inspected by FDA?
The most recent FDA inspection document on file for AVEM Labs LLC is a Form 483 dated May 21, 2025.
What did FDA cite at AVEM Labs LLC?
The regulations cited most in the observations on file for AVEM Labs LLC are 21 CFR 1271.200 (Equipment), 1 time; 21 CFR 1271.210 (Supplies and reagents), 1 time; 21 CFR 1271.230 (Process validation), 1 time.