FDA Inspection 1069353 — Depalt, Inc

Depalt, Inc — FEI 3005289267

The FDA completed an inspection of Depalt, Inc on Aug 2, 2018 in Plano, TX. 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
Aug 2, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Plano, TX (United States)