FDA Inspection 1064587 — Blazejewski Medi-Tech

Blazejewski Medi-Tech — FEI 3003058840

The FDA completed an inspection of Blazejewski Medi-Tech on Jul 6, 2018 in Sexau. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 6, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Sexau (Germany)