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FDA Inspection 912700 — Veran Medical Technologies Inc

Veran Medical Technologies Inc — FEI 3007222345

The FDA completed an inspection of Veran Medical Technologies Inc on February 4, 2015 in Saint Louis, MO. 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
February 4, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Saint Louis, MO (United States)

Facility

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FDA data resources