Company
United StatesRePharm LLC, Riverside, MO – FDA Inspections
Inspection records and compliance data for RePharm LLC in Riverside, Missouri. 3 FDA inspections on record (2 OAI), 2 Form 483s, last inspected November 15, 2023.
Company Profile
This profile covers RePharm LLC based in Riverside, Missouri, United States.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 2
- VAI
- 1
- NAI
- 0
- Form 483s
- 2
- Warning letters
- 0
First inspected July 3, 2019. Last inspected November 15, 2023.
Most cited issue areas
- Adequate number of batches on stability2 inspections
- Calibration/Inspection/Checking not done2 inspections
- Training--operations, GMPs, written procedures2 inspections
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| November 15, 2023 | VAI | Human Drugs · Drug Quality Assurance | 1224274 |
| June 25, 2021 | OAI | Human Drugs · Drug Quality Assurance | 1145918 |
| July 3, 2019 | OAI | Human Drugs · Drug Quality Assurance | 1095778 |
FDA documents
Form 483s (2)
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
RePharm LLC
FEI Number
3015474688
Address
1831 Nw Vivion Rd, Riverside, Missouri 64150, United States
Country
United States
ID: d39558e4-a44b-43c5-b75c-563dee1dd778