FDA Inspection 1167428 — Magnolia Medical Technologies, Inc.

Magnolia Medical Technologies, Inc. — FEI 3009976527

The FDA completed an inspection of Magnolia Medical Technologies, Inc. on April 6, 2022 in Seattle, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 6, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Seattle, WA (United States)