FDA Inspection 996734 — Eric Hoffer M.D.

Eric Hoffer M.D. — FEI 3012927309

The FDA completed an inspection of Eric Hoffer M.D. on Nov 17, 2016 in Lebanon, NH. 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
Nov 17, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Lebanon, NH (United States)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.