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FDA Inspection 1030120 — Ventana Medical Systems, Inc.

Ventana Medical Systems, Inc. — FEI 1000125183

The FDA completed an inspection of Ventana Medical Systems, Inc. on July 13, 2017 in Tucson, AZ. 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
July 13, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tucson, AZ (United States)

Facility

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  • 1121325 (NAI Wed Feb 26 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources