FEI 3018078670
FDA inspection history in Washington, District of Columbia, 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 Washington, District of Columbia.
Cited most
Across all site observations on file
- 21 CFR 820.20(c)Management responsibility1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.70(i)Production and process controls1
- 21 CFR 820.80(a)Receiving, in-process, and finished device acceptance1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Washington, District of Columbia
One Form 483 · 2024 · 4 observations
Latest: Form 483, Nov 6, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-11-06 | 483 Form 483 | Washington, District of Columbia | 4 | $99 |
Investigators on these documents
FEI number 3018078670 · most recent document Nov 6, 2024
About FEI 3018078670
How many FDA Form 483s has FEI 3018078670 received?
FDA Intel has 1 Form 483 on file for FEI 3018078670; the most recent is dated Nov 6, 2024.
When was FEI 3018078670 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3018078670 is a Form 483 dated Nov 6, 2024, for the site in Washington, District of Columbia.
What did FDA cite at FEI 3018078670?
The regulations cited most in the observations on file for FEI 3018078670 are 21 CFR 820.20(c) (Management responsibility), 1 time; 21 CFR 820.22 (Quality audit), 1 time; 21 CFR 820.70(i) (Production and process controls), 1 time.