University of Iowa Pharmaceuticals
FDA inspection history in Iowa City, Iowa, 2018 to 2023
- 2
- Form 483s
Every document, by year
- Form 483
2018: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Iowa City, Iowa.
- 2023One Form 483, at Iowa City, Iowa.
- 2023The longest 483 on file: 4 observations over 5 pages at Iowa City, Iowa.
Cited most
Across all University of Iowa Pharmaceuticals observations on file
- 21 CFR 211.198Complaint files2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.165(e)Testing and release for distribution1
- 21 CFR 211.42(c)(10)Design and construction features1
The complete University of Iowa Pharmaceuticals 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
Iowa City, Iowa
Two Form 483s · 2018 to 2023 · 8 observations
Latest: Form 483, Jun 22, 2023 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-06-22 | 483 Form 483 | Iowa City, Iowa | 4 | $99 |
| 2018-05-04 | 483 Form 483 | Iowa City, Iowa | 4 | $99 |
Investigators on these documents
FEI number 1918751 · most recent document Jun 22, 2023
About University of Iowa Pharmaceuticals
How many FDA Form 483s has University of Iowa Pharmaceuticals received?
FDA Intel has 2 Form 483s on file for University of Iowa Pharmaceuticals; the most recent is dated Jun 22, 2023.
When was University of Iowa Pharmaceuticals last inspected by FDA?
The most recent FDA inspection document on file for University of Iowa Pharmaceuticals is a Form 483 dated Jun 22, 2023, for the site in Iowa City, Iowa.
What did FDA cite at University of Iowa Pharmaceuticals?
The regulations cited most in the observations on file for University of Iowa Pharmaceuticals are 21 CFR 211.198 (Complaint files), 2 times; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.113 (Control of microbiological contamination), 1 time.