Velocity Production and Packaging
FDA inspection history in Tempe, Arizona, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Tempe, Arizona.
Cited most
Across all Velocity Production and Packaging observations on file
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.166(a)(3)Stability testing1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Velocity Production and Packaging file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Tempe, Arizona
One Form 483 · 2019 · 3 observations
Latest: Form 483, May 8, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-05-08 | 483 Form 483 | Tempe, Arizona | 3 | $99 |
Investigators on these documents
FEI number 3014736593 · most recent document May 8, 2019
About Velocity Production and Packaging
How many FDA Form 483s has Velocity Production and Packaging received?
FDA Intel has 1 Form 483 on file for Velocity Production and Packaging; the most recent is dated May 8, 2019.
When was Velocity Production and Packaging last inspected by FDA?
The most recent FDA inspection document on file for Velocity Production and Packaging is a Form 483 dated May 8, 2019, for the site in Tempe, Arizona.
What did FDA cite at Velocity Production and Packaging?
The regulations cited most in the observations on file for Velocity Production and Packaging are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.166(a)(3) (Stability testing), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.