FDA Inspection 824116 — TYRX Inc.

TYRX Inc. — FEI 3005619263

The FDA completed an inspection of TYRX Inc. on March 26, 2013 in Monmouth Junction, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 26, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Monmouth Junction, NJ (United States)