Maiden Biosciences
FDA inspection history in Gaithersburg, Maryland, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Gaithersburg, Maryland.
Cited most
Across all Maiden Biosciences observations on file
- 21 CFR 820.20(b)(3)Management responsibility1
- 21 CFR 820.25(b)Personnel1
The complete Maiden Biosciences file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Gaithersburg, Maryland
One Form 483 · 2022 · 2 observations
Latest: Form 483, Nov 28, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-11-28 | 483 Form 483 | Gaithersburg, Maryland | 2 | $99 |
Investigators on these documents
FEI number 3012973796 · most recent document Nov 28, 2022
About Maiden Biosciences
How many FDA Form 483s has Maiden Biosciences received?
FDA Intel has 1 Form 483 on file for Maiden Biosciences; the most recent is dated Nov 28, 2022.
When was Maiden Biosciences last inspected by FDA?
The most recent FDA inspection document on file for Maiden Biosciences is a Form 483 dated Nov 28, 2022, for the site in Gaithersburg, Maryland.
What did FDA cite at Maiden Biosciences?
The regulations cited most in the observations on file for Maiden Biosciences are 21 CFR 820.20(b)(3) (Management responsibility), 1 time; 21 CFR 820.25(b) (Personnel), 1 time.