FDA Inspection 636190 — Ora, Inc.

Ora, Inc. — FEI 3007982812

The FDA completed an inspection of Ora, Inc. on December 23, 2009 in Andover, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 23, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Andover, MA (United States)

Additional Details

Sponsor, Contract Research Organization