Hoosier, Inc
FDA inspection history in Corona, California, 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 Corona, California.
Cited most
Across all Hoosier observations on file
- 21 CFR 820.80(a)Receiving, in-process, and finished device acceptance2
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.50Purchasing controls1
- 21 CFR 820.75(a)Process validation1
The complete Hoosier file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Corona, California
One Form 483 · 2025 · 6 observations
Latest: Form 483, Aug 21, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-08-21 | 483 Form 483 | Corona, California | 6 | $99 |
Investigators on these documents
FEI number 3003058119 · most recent document Aug 21, 2025
About Hoosier, Inc
How many FDA Form 483s has Hoosier, Inc received?
FDA Intel has 1 Form 483 on file for Hoosier, Inc; the most recent is dated Aug 21, 2025.
When was Hoosier, Inc last inspected by FDA?
The most recent FDA inspection document on file for Hoosier, Inc is a Form 483 dated Aug 21, 2025, for the site in Corona, California.
What did FDA cite at Hoosier, Inc?
The regulations cited most in the observations on file for Hoosier, Inc are 21 CFR 820.80(a) (Receiving, in-process, and finished device acceptance), 2 times; 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time.