FDA Inspection 1325092 — Clario (BioClinica, Inc.)

Clario (BioClinica, Inc.) — FEI 1000103389

The FDA completed an inspection of Clario (BioClinica, Inc.) on Jun 25, 2026 in Philadelphia, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 25, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Philadelphia, PA (United States)

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