Diamondback Drugs of Delaware, LLC
FDA inspection history in Scottsdale, Arizona, 2013
- 1
- Form 483
Every document, by year
- Form 483
2013: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2013One Form 483, at Scottsdale, Arizona.
Cited most
Across all Diamondback Drugs of Delaware observations on file
- 21 CFR 211.113(b)Control of microbiological contamination2
- 21 CFR 211.42(c)Design and construction features2
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.182Equipment cleaning and use log1
- 21 CFR 211.188(b)(3)Batch production and control records1
The complete Diamondback Drugs of Delaware file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Scottsdale, Arizona
One Form 483 · 2013 · 8 observations
Latest: Form 483, May 17, 2013 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2013-05-17 | 483 Form 483 | Scottsdale, Arizona | 8 | $99 |
Investigators on these documents
FEI number 3003542383 · most recent document May 17, 2013
About Diamondback Drugs of Delaware, LLC
How many FDA Form 483s has Diamondback Drugs of Delaware, LLC received?
FDA Intel has 1 Form 483 on file for Diamondback Drugs of Delaware, LLC; the most recent is dated May 17, 2013.
When was Diamondback Drugs of Delaware, LLC last inspected by FDA?
The most recent FDA inspection document on file for Diamondback Drugs of Delaware, LLC is a Form 483 dated May 17, 2013, for the site in Scottsdale, Arizona.
What did FDA cite at Diamondback Drugs of Delaware, LLC?
The regulations cited most in the observations on file for Diamondback Drugs of Delaware, LLC are 21 CFR 211.113(b) (Control of microbiological contamination), 2 times; 21 CFR 211.42(c) (Design and construction features), 2 times; 21 CFR 211.166(a) (Stability testing), 1 time.