FDA Inspection 1099882 — Kaleo, Inc.

Kaleo, Inc. — FEI 3007135538

The FDA completed an inspection of Kaleo, Inc. on July 31, 2019 in Richmond, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 31, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Richmond, VA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)