Dynex Technologies, Inc
FDA inspection history in Chantilly, Virginia, 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 Chantilly, Virginia.
Cited most
Across all Dynex Technologies observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.50(a)Purchasing controls1
The complete Dynex Technologies file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Chantilly, Virginia
One Form 483 · 2022 · 3 observations
Latest: Form 483, Feb 18, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-02-18 | 483 Form 483 | Chantilly, Virginia | 3 | $99 |
Investigators on these documents
FEI number 1117676 · most recent document Feb 18, 2022
About Dynex Technologies, Inc
How many FDA Form 483s has Dynex Technologies, Inc received?
FDA Intel has 1 Form 483 on file for Dynex Technologies, Inc; the most recent is dated Feb 18, 2022.
When was Dynex Technologies, Inc last inspected by FDA?
The most recent FDA inspection document on file for Dynex Technologies, Inc is a Form 483 dated Feb 18, 2022, for the site in Chantilly, Virginia.
What did FDA cite at Dynex Technologies, Inc?
The regulations cited most in the observations on file for Dynex Technologies, Inc are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time; 21 CFR 820.50(a) (Purchasing controls), 1 time.