Acuity Specialty Products, Inc dba AFCO US
FDA inspection history in Chambersburg, Pennsylvania, 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 Chambersburg, Pennsylvania.
Cited most
Across all Acuity Specialty Products, Inc dba AFCO US observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.180(e)(2)General requirements1
- 21 CFR 211.192Production record review1
The complete Acuity Specialty Products, Inc dba AFCO US file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Chambersburg, Pennsylvania
One Form 483 · 2025 · 9 observations
Latest: Form 483, Mar 14, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-03-14 | 483 Form 483 | Chambersburg, Pennsylvania | 9 | $99 |
Investigators on these documents
FEI number 3006317477 · most recent document Mar 14, 2025
About Acuity Specialty Products, Inc dba AFCO US
How many FDA Form 483s has Acuity Specialty Products, Inc dba AFCO US received?
FDA Intel has 1 Form 483 on file for Acuity Specialty Products, Inc dba AFCO US; the most recent is dated Mar 14, 2025.
When was Acuity Specialty Products, Inc dba AFCO US last inspected by FDA?
The most recent FDA inspection document on file for Acuity Specialty Products, Inc dba AFCO US is a Form 483 dated Mar 14, 2025, for the site in Chambersburg, Pennsylvania.
What did FDA cite at Acuity Specialty Products, Inc dba AFCO US?
The regulations cited most in the observations on file for Acuity Specialty Products, Inc dba AFCO US are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.166(a) (Stability testing), 1 time.