FDA Inspection 1123874 — B-ONE ORTHO, CORP.

B-ONE ORTHO, CORP. — FEI 3015259876

The FDA completed an inspection of B-ONE ORTHO, CORP. on Jan 15, 2020 in Cedar Knolls, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jan 15, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Cedar Knolls, NJ (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.