FDA Inspection 655208 — Ondine Research Laboratories, Inc.

Ondine Research Laboratories, Inc. — FEI 3006845489

The FDA completed an inspection of Ondine Research Laboratories, Inc. on March 16, 2010 in Bothell, WA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
March 16, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Bothell, WA (United States)

Additional Details

Sponsor, Contract Research Organization