FDA Inspection 771891 — Acu Med Inc

Acu Med Inc — FEI 3000530535

The FDA completed an inspection of Acu Med Inc on Mar 7, 2012 in Burbank, CA. 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
Mar 7, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Burbank, CA (United States)

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