FDA Inspection 1172026 — The Flexite Company

The Flexite Company — FEI 2432071

The FDA completed an inspection of The Flexite Company on Jun 1, 2022 in Mineola, NY. 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 1, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Mineola, NY (United States)