FDA Inspection 643708 — Clario (BioClinica, Inc.)

Clario (BioClinica, Inc.) — FEI 1000103389

The FDA completed an inspection of Clario (BioClinica, Inc.) on Feb 5, 2010 in Philadelphia, PA. 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
Feb 5, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Philadelphia, PA (United States)

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