Gehring-Montgomery, Inc.
FDA inspection history in Warminster, 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 Warminster, Pennsylvania.
Cited most
Across all Gehring-Montgomery observations on file
- 21 CFR 211.25Personnel qualifications1
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures1
The complete Gehring-Montgomery file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Warminster, Pennsylvania
One Form 483 · 2024 · 3 observations
Latest: Form 483, Feb 9, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-02-09 | 483 Form 483 | Warminster, Pennsylvania | 3 | $99 |
Investigators on these documents
FEI number 3000214933 · most recent document Feb 9, 2024
About Gehring-Montgomery, Inc.
How many FDA Form 483s has Gehring-Montgomery, Inc. received?
FDA Intel has 1 Form 483 on file for Gehring-Montgomery, Inc.; the most recent is dated Feb 9, 2024.
When was Gehring-Montgomery, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Gehring-Montgomery, Inc. is a Form 483 dated Feb 9, 2024, for the site in Warminster, Pennsylvania.
What did FDA cite at Gehring-Montgomery, Inc.?
The regulations cited most in the observations on file for Gehring-Montgomery, Inc. are 21 CFR 211.25 (Personnel qualifications), 1 time; 21 CFR 211.84 (Testing and approval or rejection of components, drug product containers, and closures), 1 time.