FDA Inspection 1210632 — Ora, Inc.

Ora, Inc. — FEI 3007982812

The FDA completed an inspection of Ora, Inc. on June 28, 2023 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
June 28, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Andover, MA (United States)

Additional Details

Sponsor, Contract Research Organization