FDA inspection
MeKo Manufacturing e.K.: FDA inspection ending Feb 21, 2019
FDA inspection 1080539 · Voluntary Action Indicated (VAI) · Sarstedt
Key facts
| Inspection ID | 1080539 |
|---|---|
| Firm | MeKo Manufacturing e.K. |
| FEI number | 3009937642 |
| Address | Im Kirchenfelde 12-14 |
| City | Sarstedt |
| Country | Germany |
| Fiscal year | 2019 |
| Inspection end date | Feb 21, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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