FDA Inspection 913280 — Accu-Fab, Inc

Accu-Fab, Inc — FEI 3003880927

The FDA completed an inspection of Accu-Fab, Inc on Feb 10, 2015 in Raleigh, NC. 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
Feb 10, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Raleigh, NC (United States)

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