FDA Inspection 1039905 — Altimate Medical, Inc.

Altimate Medical, Inc. — FEI 2183634

The FDA completed an inspection of Altimate Medical, Inc. on Nov 15, 2017 in Morton, MN. 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
Nov 15, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Morton, MN (United States)

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