QPharma AB — FDA Facility Profile
QPharma AB is an FDA-registered facility (FEI 3004620701) located in Skane S-21215, SE. Registered operations: ANALYSIS; LABEL; MANUFACTURE; PACK. RegDataLab tracks 5 FDA inspections at this facility.
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What FDA found at this site
- Latest inspection
- May 12, 2023: Voluntary Action Indicated (VAI)
- Inspections on record
- 5 (3 VAI, 2 NAI)
- Last OAI inspection
- None on record
- Warning letters
- None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
- Import refusals
- 1
Inspections and what FDA cited
| Date | Result | What FDA cited |
|---|---|---|
| May 12, 2023 | Voluntary Action Indicated (VAI) | No citations listed |
| Mar 31, 2023 | No Action Indicated (NAI) | No citations listed |
| Nov 23, 2017 | Voluntary Action Indicated (VAI) | No citations listed |
| Jun 1, 2016 | No Action Indicated (NAI) | No citations listed |
| Mar 27, 2014 | Voluntary Action Indicated (VAI) | Actual vs. theoretical yields not determined (21 CFR 211.103) |
Facility details
- Company
- QPharma AB
- Location
- Skane S-21215 (SE)
- Registration Expires
- Dec 31, 2027
- Operations
- ANALYSIS; LABEL; MANUFACTURE; PACK
- Source
- decrs