FDA Inspection 700329 — Advent Medical Products, Inc.

Advent Medical Products, Inc. — FEI 3005110371

The FDA completed an inspection of Advent Medical Products, Inc. on November 16, 2010 in Cambridge, MA. 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
November 16, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Cambridge, MA (United States)