FDA Inspection 668090 — TYRX Inc.

TYRX Inc. — FEI 3005619263

The FDA completed an inspection of TYRX Inc. on Jun 22, 2010 in Monmouth Junction, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 22, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Monmouth Junction, NJ (United States)

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