AEI Technologies, Inc
FDA inspection history in Pittsburgh, Pennsylvania, 2015
- 1
- Form 483
Every document, by year
- Form 483
2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Pittsburgh, Pennsylvania.
Cited most
Across all AEI Technologies observations on file
- 21 CFR 820.22Quality audit2
- 21 CFR 8201
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.198(b)Complaint files1
- 21 CFR 820.20(b)Management responsibility1
The complete AEI Technologies file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Pittsburgh, Pennsylvania
One Form 483 · 2015 · 8 observations
Latest: Form 483, Sep 18, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-09-18 | 483 Form 483 | Pittsburgh, Pennsylvania | 8 | $99 |
Investigators on these documents
FEI number 3004055954 · most recent document Sep 18, 2015
About AEI Technologies, Inc
How many FDA Form 483s has AEI Technologies, Inc received?
FDA Intel has 1 Form 483 on file for AEI Technologies, Inc; the most recent is dated Sep 18, 2015.
When was AEI Technologies, Inc last inspected by FDA?
The most recent FDA inspection document on file for AEI Technologies, Inc is a Form 483 dated Sep 18, 2015, for the site in Pittsburgh, Pennsylvania.
What did FDA cite at AEI Technologies, Inc?
The regulations cited most in the observations on file for AEI Technologies, Inc are 21 CFR 820.22 (Quality audit), 2 times; 21 CFR 820, 1 time; 21 CFR 820.100(a) (Corrective and preventive action), 1 time.