FDA inspection
QPharma AB: FDA inspection ending Dec 15, 2017
FDA inspection 1036638 · Voluntary Action Indicated (VAI) · Malmo
Key facts
| Inspection ID | 1036638 |
|---|---|
| Firm | QPharma AB |
| FEI number | 3004620701 |
| Address | Agnselundsvagen 27 |
| City | Malmo |
| Fiscal year | 2018 |
| Inspection end date | Dec 15, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation|Compliance: Med Devices|Compliance: Medical Devices|New Drug Evaluation |
| Product type | Devices, Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data