FDA Inspection 880791 — Dale A. Presser

Dale A. Presser — FEI 3010836505

The FDA completed an inspection of Dale A. Presser on Jun 4, 2014 in Covington, LA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 4, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Covington, LA (United States)

Additional Details

Clinical Investigator (CI)