FDA Inspection 777355 — OraSure Technologies, Inc.

OraSure Technologies, Inc. — FEI 2528909

The FDA completed an inspection of OraSure Technologies, Inc. on May 9, 2012 in Bethlehem, PA. 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
May 9, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Bethlehem, PA (United States)