FDA Inspection 935768 — Radiology Information Systems, Inc.

Radiology Information Systems, Inc. — FEI 3002952981

The FDA completed an inspection of Radiology Information Systems, Inc. on Jul 15, 2015 in Dulles, VA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 15, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Dulles, VA (United States)

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