FDA Inspection 1034313 — BD Medical

BD Medical — FEI 1920898

The FDA completed an inspection of BD Medical on November 8, 2017 in Holdrege, NE. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 8, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Holdrege, NE (United States)