FDA Inspection 668090 — TYRX Inc.

TYRX Inc. — FEI 3005619263

The FDA completed an inspection of TYRX Inc. on June 22, 2010 in Monmouth Junction, NJ. 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 22, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Monmouth Junction, NJ (United States)