ALR Technologies
FDA inspection history in North Chesterfield, Virginia, 2016
- 1
- Form 483
Every document, by year
- Form 483
2016: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at North Chesterfield, Virginia.
Cited most
Across all ALR Technologies observations on file
- 21 CFR 820.20(a)Management responsibility2
- 21 CFR 820.50Purchasing controls2
- 21 CFR 820.100(b)Corrective and preventive action1
- 21 CFR 820.181Device master record1
- 21 CFR 820.198(a)Complaint files1
The complete ALR Technologies file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
North Chesterfield, Virginia
One Form 483 · 2016 · 13 observations
Latest: Form 483, Mar 22, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-03-22 | 483 Form 483 | North Chesterfield, Virginia | 13 | $99 |
Investigators on these documents
FEI number 3009349614 · most recent document Mar 22, 2016
About ALR Technologies
How many FDA Form 483s has ALR Technologies received?
FDA Intel has 1 Form 483 on file for ALR Technologies; the most recent is dated Mar 22, 2016.
When was ALR Technologies last inspected by FDA?
The most recent FDA inspection document on file for ALR Technologies is a Form 483 dated Mar 22, 2016, for the site in North Chesterfield, Virginia.
What did FDA cite at ALR Technologies?
The regulations cited most in the observations on file for ALR Technologies are 21 CFR 820.20(a) (Management responsibility), 2 times; 21 CFR 820.50 (Purchasing controls), 2 times; 21 CFR 820.100(b) (Corrective and preventive action), 1 time.