FDA inspection
BIOTECH EUROPE MEDITECH Inc. Ltd: FDA inspection ending Apr 14, 2022
FDA inspection 1167365 · Voluntary Action Indicated (VAI) · Roscommon
Key facts
| Inspection ID | 1167365 |
|---|---|
| Firm | BIOTECH EUROPE MEDITECH Inc. Ltd |
| FEI number | 3016942176 |
| Address | Af 2, Ida Business & Technology Park, Gallowstown |
| City | Roscommon |
| Country | Ireland |
| Fiscal year | 2022 |
| Inspection end date | Apr 14, 2022 |
| Classification | Voluntary Action Indicated (VAI) |
| 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