FDA Inspection 1100116 — Almitech, Inc.

Almitech, Inc. — FEI 3005562016

The FDA completed an inspection of Almitech, Inc. on Apr 18, 2019 in Bellmore, NY. 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
Apr 18, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Bellmore, NY (United States)

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