FDA Inspection 1276112 — Centerline Biomedical Inc

Centerline Biomedical Inc — FEI 3012154226

The FDA completed an inspection of Centerline Biomedical Inc on Jul 2, 2025 in Cleveland, OH. 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
Jul 2, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Cleveland, OH (United States)

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