FDA Inspection 1247593 — Mauna Kea Technologies

Mauna Kea Technologies — FEI 3004542960

The FDA completed an inspection of Mauna Kea Technologies on Jul 4, 2024 in Paris. 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 4, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Paris (France)