FDA Inspection 972327 — Kevin Waltz, OD, MD

Kevin Waltz, OD, MD — FEI 3009453953

The FDA completed an inspection of Kevin Waltz, OD, MD on May 17, 2016 in Indianapolis, IN. 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
May 17, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Indianapolis, IN (United States)

Additional Details

Clinical Investigator (CI)