HUBOT, INC.
FDA inspection history in SOUTH BEND, Indiana, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at SOUTH BEND, Indiana.
Cited most
Across all HUBOT observations on file
- 21 CFR 211.84(b)Testing and approval or rejection of components, drug product containers, and closures1
The complete HUBOT file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
SOUTH BEND, Indiana
One Form 483 · 2024 · 1 observation
Latest: Form 483, Nov 8, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-11-08 | 483 Form 483 | SOUTH BEND, Indiana | 1 | $99 |
Investigators on these documents
FEI number 3015177815 · most recent document Nov 8, 2024
About HUBOT, INC.
How many FDA Form 483s has HUBOT, INC. received?
FDA Intel has 1 Form 483 on file for HUBOT, INC.; the most recent is dated Nov 8, 2024.
When was HUBOT, INC. last inspected by FDA?
The most recent FDA inspection document on file for HUBOT, INC. is a Form 483 dated Nov 8, 2024, for the site in SOUTH BEND, Indiana.
What did FDA cite at HUBOT, INC.?
The regulations cited most in the observations on file for HUBOT, INC. are 21 CFR 211.84(b) (Testing and approval or rejection of components, drug product containers, and closures), 1 time.