OL PHARMA TECH, LLC
FDA inspection history in madison heights, Michigan, 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 madison heights, Michigan.
Cited most
Across all OL PHARMA TECH observations on file
- 21 CFR 211.22(a)Responsibilities of quality control unit2
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.188Batch production and control records1
The complete OL PHARMA TECH file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
madison heights, Michigan
One Form 483 · 2024 · 9 observations
Latest: Form 483, Jul 22, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-07-22 | 483 Form 483 | madison heights, Michigan | 9 | $99 |
Investigators on these documents
FEI number 3017408112 · most recent document Jul 22, 2024
About OL PHARMA TECH, LLC
How many FDA Form 483s has OL PHARMA TECH, LLC received?
FDA Intel has 1 Form 483 on file for OL PHARMA TECH, LLC; the most recent is dated Jul 22, 2024.
When was OL PHARMA TECH, LLC last inspected by FDA?
The most recent FDA inspection document on file for OL PHARMA TECH, LLC is a Form 483 dated Jul 22, 2024, for the site in madison heights, Michigan.
What did FDA cite at OL PHARMA TECH, LLC?
The regulations cited most in the observations on file for OL PHARMA TECH, LLC are 21 CFR 211.22(a) (Responsibilities of quality control unit), 2 times; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160(b) (General requirements), 1 time.