FDA inspection
Apotek Production & Laboratorier AB: FDA inspection ending Dec 13, 2018
FDA inspection 1080977 · No Action Indicated (NAI) · Umea
Key facts
| Inspection ID | 1080977 |
|---|---|
| Firm | Apotek Production & Laboratorier AB |
| FEI number | 3003766921 |
| Address | Formvagen 5B |
| City | Umea |
| Country | Sweden |
| Fiscal year | 2019 |
| Inspection end date | Dec 13, 2018 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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