FDA Inspection 913796 — Titertek Instruments Inc

Titertek Instruments Inc — FEI 1028229

The FDA completed an inspection of Titertek Instruments Inc on Feb 10, 2015 in Huntsville, AL. 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
Feb 10, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Huntsville, AL (United States)