Forge Medical Inc
FDA inspection history in Bethlehem, Pennsylvania, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Bethlehem, Pennsylvania.
Cited most
Across all Forge Medical observations on file
- 21 CFR 820.100(b)Corrective and preventive action1
- 21 CFR 820.181Device master record1
- 21 CFR 820.25(b)Personnel1
- 21 CFR 820.50(a)(1)Purchasing controls1
- 21 CFR 820.70(b)Production and process controls1
The complete Forge Medical file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Bethlehem, Pennsylvania
One Form 483 · 2018 · 5 observations
Latest: Form 483, Jul 18, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-07-18 | 483 Form 483 | Bethlehem, Pennsylvania | 5 | $99 |
Investigators on these documents
FEI number 3009595977 · most recent document Jul 18, 2018
About Forge Medical Inc
How many FDA Form 483s has Forge Medical Inc received?
FDA Intel has 1 Form 483 on file for Forge Medical Inc; the most recent is dated Jul 18, 2018.
When was Forge Medical Inc last inspected by FDA?
The most recent FDA inspection document on file for Forge Medical Inc is a Form 483 dated Jul 18, 2018, for the site in Bethlehem, Pennsylvania.
What did FDA cite at Forge Medical Inc?
The regulations cited most in the observations on file for Forge Medical Inc are 21 CFR 820.100(b) (Corrective and preventive action), 1 time; 21 CFR 820.181 (Device master record), 1 time; 21 CFR 820.25(b) (Personnel), 1 time.