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Action Products, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K811528RADIATION BOLUSJuly 10, 1981
K801694FLOTATION PAD FOR OPERATING TABLEAugust 27, 1980