FDA Inspection 1056872 — Donald Heck

Donald Heck — FEI 3014383242

The FDA completed an inspection of Donald Heck on Jun 7, 2018 in Winston Salem, NC. 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
Jun 7, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Winston Salem, NC (United States)

Additional Details

Clinical Investigator (CI)