FDA Inspection 1034313 — BD Medical

BD Medical — FEI 1920898

The FDA completed an inspection of BD Medical on Nov 8, 2017 in Holdrege, NE. 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
Nov 8, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Holdrege, NE (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.