FDA Inspection 1239273 — Blue Ortho

Blue Ortho — FEI 3008027912

The FDA completed an inspection of Blue Ortho on Apr 11, 2024 in Meylan. 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
Apr 11, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Meylan (France)