Advanced Orthogonal Equipment, Incorporated

FDA Regulatory Profile

Advanced Orthogonal Equipment, Incorporated appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1809-2013, Class II) was initiated on March 6, 2013.

Summary

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

Recent Recalls

NumberClassProductDate
Z-1809-2013Class IIAdvanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed ChiropractorMarch 6, 2013