FHC, Inc
FDA inspection history in Greenville, Pennsylvania, 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 Greenville, Pennsylvania.
Cited most
Across all FHC observations on file
- 21 CFR 820.30(g)Design controls2
- 21 CFR 8201
- 21 CFR 820.20(b)Management responsibility1
- 21 CFR 820.70(a)Production and process controls1
The complete FHC file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Greenville, Pennsylvania
One Form 483 · 2024 · 4 observations
Latest: Form 483, Nov 26, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-11-26 | 483 Form 483 | Greenville, Pennsylvania | 4 | $99 |
Investigators on these documents
FEI number 3005161223 · most recent document Nov 26, 2024
About FHC, Inc
How many FDA Form 483s has FHC, Inc received?
FDA Intel has 1 Form 483 on file for FHC, Inc; the most recent is dated Nov 26, 2024.
When was FHC, Inc last inspected by FDA?
The most recent FDA inspection document on file for FHC, Inc is a Form 483 dated Nov 26, 2024, for the site in Greenville, Pennsylvania.
What did FDA cite at FHC, Inc?
The regulations cited most in the observations on file for FHC, Inc are 21 CFR 820.30(g) (Design controls), 2 times; 21 CFR 820, 1 time; 21 CFR 820.20(b) (Management responsibility), 1 time.