FDA Inspection 1246506 — ERCHINGER

ERCHINGER — FEI 3002807421

The FDA completed an inspection of ERCHINGER on Jun 4, 2024 in Tuttlingen. 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
Jun 4, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Tuttlingen (Germany)