FDA Inspection 935383 — Fisher Diagnostics

Fisher Diagnostics — FEI 1181121

The FDA completed an inspection of Fisher Diagnostics on July 21, 2015 in Middletown, 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
July 21, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Middletown, VA (United States)