FDA Inspection 886377 — Magnolia Medical Technologies, Inc.

Magnolia Medical Technologies, Inc. — FEI 3009976527

The FDA completed an inspection of Magnolia Medical Technologies, Inc. on Jun 17, 2014 in Seattle, WA. 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
Jun 17, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Seattle, WA (United States)

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