FDA Inspection 793599 — Abryrx, Inc.

Abryrx, Inc. — FEI 3005972619

The FDA completed an inspection of Abryrx, Inc. on July 6, 2012 in Irvington, NY. 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
July 6, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Irvington, NY (United States)

Additional Details

Sponsor, Contract Research Organization