FDA inspection
Kitron AB: FDA inspection ending Dec 13, 2018
FDA inspection 1074723 · Official Action Indicated (OAI) · Jonkoping
Key facts
| Inspection ID | 1074723 |
|---|---|
| Firm | Kitron AB |
| FEI number | 3009834076 |
| Address | Mobelvagen 5 |
| City | Jonkoping |
| Country | Sweden |
| Fiscal year | 2019 |
| Inspection end date | Dec 13, 2018 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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