DA BOMB LLC
FDA inspection history in Minneapolis, Minnesota, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Minneapolis, Minnesota.
Cited most
Across all DA BOMB observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.165(a)Testing and release for distribution1
- 21 CFR 211.22(a)Responsibilities of quality control unit1
- 21 CFR 211.84(d)(1)Testing and approval or rejection of components, drug product containers, and closures1
The complete DA BOMB file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Minneapolis, Minnesota
One Form 483 · 2025 · 4 observations
Latest: Form 483, May 5, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-05-05 | 483 Form 483 | Minneapolis, Minnesota | 4 | $99 |
Investigators on these documents
FEI number 3014647198 · most recent document May 5, 2025
About DA BOMB LLC
How many FDA Form 483s has DA BOMB LLC received?
FDA Intel has 1 Form 483 on file for DA BOMB LLC; the most recent is dated May 5, 2025.
When was DA BOMB LLC last inspected by FDA?
The most recent FDA inspection document on file for DA BOMB LLC is a Form 483 dated May 5, 2025, for the site in Minneapolis, Minnesota.
What did FDA cite at DA BOMB LLC?
The regulations cited most in the observations on file for DA BOMB LLC are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.165(a) (Testing and release for distribution), 1 time; 21 CFR 211.22(a) (Responsibilities of quality control unit), 1 time.