CO-AX Technology Inc
FDA inspection history in Solon, Ohio, 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 Solon, Ohio.
Cited most
Across all CO-AX Technology observations on file
- 21 CFR 820.50(a)(2)Purchasing controls2
- 21 CFR 820.90(a)Nonconforming product2
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.72(a)Inspection, measuring, and test equipment1
The complete CO-AX Technology file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Solon, Ohio
One Form 483 · 2023 · 9 observations
Latest: Form 483, Aug 2, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-08-02 | 483 Form 483 | Solon, Ohio | 9 | $99 |
Investigators on these documents
FEI number 3013413442 · most recent document Aug 2, 2023
About CO-AX Technology Inc
How many FDA Form 483s has CO-AX Technology Inc received?
FDA Intel has 1 Form 483 on file for CO-AX Technology Inc; the most recent is dated Aug 2, 2023.
When was CO-AX Technology Inc last inspected by FDA?
The most recent FDA inspection document on file for CO-AX Technology Inc is a Form 483 dated Aug 2, 2023, for the site in Solon, Ohio.
What did FDA cite at CO-AX Technology Inc?
The regulations cited most in the observations on file for CO-AX Technology Inc are 21 CFR 820.50(a)(2) (Purchasing controls), 2 times; 21 CFR 820.90(a) (Nonconforming product), 2 times; 21 CFR 820.100(a) (Corrective and preventive action), 1 time.