FDA Inspection 1004836 — EPOCAL INC

EPOCAL INC — FEI 3012817228

The FDA completed an inspection of EPOCAL INC on Dec 15, 2016 in Ottawa. 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
Dec 15, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Ottawa (Canada)

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