Upsher Smith Laboratories, Inc.
FDA inspection history in Plymouth, Minnesota, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Plymouth, Minnesota.
Cited most
Across all Upsher Smith Laboratories observations on file
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Upsher Smith Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Plymouth, Minnesota
One Form 483 · 2018 · 1 observation
Latest: Form 483, Dec 19, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-12-19 | 483 Form 483 | Plymouth, Minnesota | 1 | $99 |
Investigators on these documents
Courtney R. Ingalsbe (1)Ross J. Grigsby (1)Scott A. Golladay (1)
FEI number 2123200 · most recent document Dec 19, 2018
About Upsher Smith Laboratories, Inc.
How many FDA Form 483s has Upsher Smith Laboratories, Inc. received?
FDA Intel has 1 Form 483 on file for Upsher Smith Laboratories, Inc.; the most recent is dated Dec 19, 2018.
When was Upsher Smith Laboratories, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Upsher Smith Laboratories, Inc. is a Form 483 dated Dec 19, 2018, for the site in Plymouth, Minnesota.
What did FDA cite at Upsher Smith Laboratories, Inc.?
The regulations cited most in the observations on file for Upsher Smith Laboratories, Inc. are 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.