Stoner Incorporated
FDA inspection history in Quarryville, Pennsylvania, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Quarryville, Pennsylvania.
Cited most
Across all Stoner Incorporated observations on file
- 21 CFR 820.181Device master record1
- 21 CFR 820.20(b)(3)(i)Management responsibility1
The complete Stoner Incorporated file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Quarryville, Pennsylvania
One Form 483 · 2023 · 2 observations
Latest: Form 483, Nov 15, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-11-15 | 483 Form 483 | Quarryville, Pennsylvania | 2 | $99 |
Investigators on these documents
FEI number 3000538043 · most recent document Nov 15, 2023
About Stoner Incorporated
How many FDA Form 483s has Stoner Incorporated received?
FDA Intel has 1 Form 483 on file for Stoner Incorporated; the most recent is dated Nov 15, 2023.
When was Stoner Incorporated last inspected by FDA?
The most recent FDA inspection document on file for Stoner Incorporated is a Form 483 dated Nov 15, 2023, for the site in Quarryville, Pennsylvania.
What did FDA cite at Stoner Incorporated?
The regulations cited most in the observations on file for Stoner Incorporated are 21 CFR 820.181 (Device master record), 1 time; 21 CFR 820.20(b)(3)(i) (Management responsibility), 1 time.