ProMed Pharma, LLC
FDA inspection history in Plymouth, Minnesota, 2023 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2023: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023–24Two Form 483s, at Plymouth, Minnesota.
- 2024The longest 483 on file: 1 observation over 3 pages at Plymouth, Minnesota.
Cited most
Across all ProMed Pharma observations on file
- 21 CFR 211.180(e)(2)General requirements1
- 21 CFR 820.100(a)Corrective and preventive action1
The complete ProMed Pharma file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Plymouth, Minnesota
Two Form 483s · 2023 to 2024 · 2 observations
Latest: Form 483, Feb 21, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-02-21 | 483 Form 483 | Plymouth, Minnesota | 1 | $99 |
| 2023-10-17 | 483 Form 483 | Plymouth, Minnesota | 1 | $99 |
Investigators on these documents
FEI number 3003335547 · most recent document Feb 21, 2024
About ProMed Pharma, LLC
How many FDA Form 483s has ProMed Pharma, LLC received?
FDA Intel has 2 Form 483s on file for ProMed Pharma, LLC; the most recent is dated Feb 21, 2024.
When was ProMed Pharma, LLC last inspected by FDA?
The most recent FDA inspection document on file for ProMed Pharma, LLC is a Form 483 dated Feb 21, 2024, for the site in Plymouth, Minnesota.
What did FDA cite at ProMed Pharma, LLC?
The regulations cited most in the observations on file for ProMed Pharma, LLC are 21 CFR 211.180(e)(2) (General requirements), 1 time; 21 CFR 820.100(a) (Corrective and preventive action), 1 time.