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FDA Inspection 881285 — Amplion Clinical Communications, Inc.

Amplion Clinical Communications, Inc. — FEI 3009164985

The FDA completed an inspection of Amplion Clinical Communications, Inc. on June 5, 2014 in Nashville, TN. 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
June 5, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Nashville, TN (United States)

Facility

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Recent compliance actions

FDA data resources