Johnson Medtech LLC
FDA inspection history in Vandalia, Ohio, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Vandalia, Ohio.
Cited most
Across all Johnson Medtech observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.184Device history record1
- 21 CFR 820.70(a)Production and process controls1
- 21 CFR 820.75(a)Process validation1
- 21 CFR 820.86Acceptance status1
The complete Johnson Medtech file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Vandalia, Ohio
One Form 483 · 2022 · 6 observations
Latest: Form 483, Dec 8, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-12-08 | 483 Form 483 | Vandalia, Ohio | 6 | $99 |
Investigators on these documents
FEI number 3013522941 · most recent document Dec 8, 2022
About Johnson Medtech LLC
How many FDA Form 483s has Johnson Medtech LLC received?
FDA Intel has 1 Form 483 on file for Johnson Medtech LLC; the most recent is dated Dec 8, 2022.
When was Johnson Medtech LLC last inspected by FDA?
The most recent FDA inspection document on file for Johnson Medtech LLC is a Form 483 dated Dec 8, 2022, for the site in Vandalia, Ohio.
What did FDA cite at Johnson Medtech LLC?
The regulations cited most in the observations on file for Johnson Medtech LLC are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.184 (Device history record), 1 time; 21 CFR 820.70(a) (Production and process controls), 1 time.