FDA Inspection 1027435 — Conforma Laboratories Inc

Conforma Laboratories Inc — FEI 1000029583

The FDA completed an inspection of Conforma Laboratories Inc on August 7, 2017 in Norfolk, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Norfolk, VA (United States)