ATZ Manufacturing
FDA inspection history in Marshall, Minnesota, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Marshall, Minnesota.
Cited most
Across all ATZ Manufacturing observations on file
- 21 CFR 8301
- 21 CFR 801.20(a)Label to bear a unique device identifier1
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.184Device history record1
- 21 CFR 820.198(a)Complaint files1
The complete ATZ Manufacturing file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Marshall, Minnesota
One Form 483 · 2025 · 9 observations
Latest: Form 483, Jul 24, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-07-24 | 483 Form 483 | Marshall, Minnesota | 9 | $99 |
Investigators on these documents
FEI number 3014653196 · most recent document Jul 24, 2025
About ATZ Manufacturing
How many FDA Form 483s has ATZ Manufacturing received?
FDA Intel has 1 Form 483 on file for ATZ Manufacturing; the most recent is dated Jul 24, 2025.
When was ATZ Manufacturing last inspected by FDA?
The most recent FDA inspection document on file for ATZ Manufacturing is a Form 483 dated Jul 24, 2025, for the site in Marshall, Minnesota.
What did FDA cite at ATZ Manufacturing?
The regulations cited most in the observations on file for ATZ Manufacturing are 21 CFR 830, 1 time; 21 CFR 801.20(a) (Label to bear a unique device identifier), 1 time; 21 CFR 820.100(a) (Corrective and preventive action), 1 time.