FDA Inspection 643708 — Clario Inc.

Clario Inc. — FEI 1000103389

The FDA completed an inspection of Clario Inc. on February 5, 2010 in Philadelphia, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 5, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Philadelphia, PA (United States)