FDA Inspection 1019852 — Accel Inc

Accel Inc — FEI 3003042119

The FDA completed an inspection of Accel Inc on Jun 15, 2017 in New Albany, OH. 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 15, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
New Albany, OH (United States)

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