Modavar Pharmaceuticals
FDA inspection history in Frederick, Maryland, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Frederick, Maryland.
Cited most
Across all Modavar Pharmaceuticals observations on file
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.111Time limitations on production1
- 21 CFR 211.166Stability testing1
- 21 CFR 211.192Production record review1
The complete Modavar Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Frederick, Maryland
One Form 483 · 2023 · 8 observations
Latest: Form 483, Jan 27, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-01-27 | 483 Form 483 | Frederick, Maryland | 8 | $99 |
Investigators on these documents
FEI number 3014525970 · most recent document Jan 27, 2023
About Modavar Pharmaceuticals
How many FDA Form 483s has Modavar Pharmaceuticals received?
FDA Intel has 1 Form 483 on file for Modavar Pharmaceuticals; the most recent is dated Jan 27, 2023.
When was Modavar Pharmaceuticals last inspected by FDA?
The most recent FDA inspection document on file for Modavar Pharmaceuticals is a Form 483 dated Jan 27, 2023, for the site in Frederick, Maryland.
What did FDA cite at Modavar Pharmaceuticals?
The regulations cited most in the observations on file for Modavar Pharmaceuticals are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.111 (Time limitations on production), 1 time.