FDA Inspection 547235 — WHPM Inc.

WHPM Inc. — FEI 3003102569

The FDA completed an inspection of WHPM Inc. on Nov 12, 2008 in Irwindale, CA. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Nov 12, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Irwindale, CA (United States)

Additional Details

Sponsor, Contract Research Organization