FEI 3014833750
FDA inspection history in Durham, North Carolina, 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 Durham, North Carolina.
Cited most
Across all site observations on file
- 21 CFR 820.120(b)Device labeling1
- 21 CFR 820.184Device history record1
- 21 CFR 820.30(f)Design controls1
- 21 CFR 820.50(a)Purchasing controls1
- 21 CFR 820.70(b)Production and process controls1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Durham, North Carolina
One Form 483 · 2024 · 7 observations
Latest: Form 483, Jun 14, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-06-14 | 483 Form 483 | Durham, North Carolina | 7 | $99 |
Investigators on these documents
FEI number 3014833750 · most recent document Jun 14, 2024
About FEI 3014833750
How many FDA Form 483s has FEI 3014833750 received?
FDA Intel has 1 Form 483 on file for FEI 3014833750; the most recent is dated Jun 14, 2024.
When was FEI 3014833750 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3014833750 is a Form 483 dated Jun 14, 2024, for the site in Durham, North Carolina.
What did FDA cite at FEI 3014833750?
The regulations cited most in the observations on file for FEI 3014833750 are 21 CFR 820.120(b) (Device labeling), 1 time; 21 CFR 820.184 (Device history record), 1 time; 21 CFR 820.30(f) (Design controls), 1 time.