FDA Inspection 865920 — Kaleo, Inc.

Kaleo, Inc. — FEI 3007135538

The FDA completed an inspection of Kaleo, Inc. on February 11, 2014 in Richmond, VA. 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 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Richmond, VA (United States)