Active Intelligence, LLC
FDA inspection history in Cherryville, North Carolina, 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 Cherryville, North Carolina.
Cited most
Across all Active Intelligence observations on file
- 21 CFR 211.122(d)Materials examination and usage criteria1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.180(e)General requirements1
- 21 CFR 211.80(b)General requirements1
The complete Active Intelligence file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Cherryville, North Carolina
One Form 483 · 2024 · 4 observations
Latest: Form 483, Mar 8, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-03-08 | 483 Form 483 | Cherryville, North Carolina | 4 | $99 |
Investigators on these documents
FEI number 3014556381 · most recent document Mar 8, 2024
About Active Intelligence, LLC
How many FDA Form 483s has Active Intelligence, LLC received?
FDA Intel has 1 Form 483 on file for Active Intelligence, LLC; the most recent is dated Mar 8, 2024.
When was Active Intelligence, LLC last inspected by FDA?
The most recent FDA inspection document on file for Active Intelligence, LLC is a Form 483 dated Mar 8, 2024, for the site in Cherryville, North Carolina.
What did FDA cite at Active Intelligence, LLC?
The regulations cited most in the observations on file for Active Intelligence, LLC are 21 CFR 211.122(d) (Materials examination and usage criteria), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time; 21 CFR 211.180(e) (General requirements), 1 time.