FDA Inspection 1103034 — Acme Portable Machines Inc

Acme Portable Machines Inc — FEI 1000493900

The FDA completed an inspection of Acme Portable Machines Inc on Jul 18, 2019 in Azusa, 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
Jul 18, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Azusa, CA (United States)

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