Tobii Assistive Technology, Inc.

FDA Regulatory Profile

Tobii Assistive Technology, Inc. appears in FDA public data with 1 recall, 0 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0766-2013, Class II) was initiated on January 14, 2013.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
2
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0766-2013Class IIP10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobii P10 DeviceJanuary 14, 2013