FDA Inspection 1268308 — BIOTECH EUROPE MEDITECH Inc. Ltd

BIOTECH EUROPE MEDITECH Inc. Ltd — FEI 3016942176

The FDA completed an inspection of BIOTECH EUROPE MEDITECH Inc. Ltd on March 26, 2025 in Roscommon. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 26, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Roscommon (Ireland)