Upsher-Smith Laboratories, LLC
FDA inspection history in Denver, Colorado, 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 Denver, Colorado.
Cited most
Across all Upsher-Smith Laboratories observations on file
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.192Production record review1
The complete Upsher-Smith Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Denver, Colorado
One Form 483 · 2019 · 2 observations
Latest: Form 483, Nov 7, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-11-07 | 483 Form 483 | Denver, Colorado | 2 | $99 |
Investigators on these documents
FEI number 1719991 · most recent document Nov 7, 2019
About Upsher-Smith Laboratories, LLC
How many FDA Form 483s has Upsher-Smith Laboratories, LLC received?
FDA Intel has 1 Form 483 on file for Upsher-Smith Laboratories, LLC; the most recent is dated Nov 7, 2019.
When was Upsher-Smith Laboratories, LLC last inspected by FDA?
The most recent FDA inspection document on file for Upsher-Smith Laboratories, LLC is a Form 483 dated Nov 7, 2019, for the site in Denver, Colorado.
What did FDA cite at Upsher-Smith Laboratories, LLC?
The regulations cited most in the observations on file for Upsher-Smith Laboratories, LLC are 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.192 (Production record review), 1 time.