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Ind Diagnostics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K113506
IND ONE STEP OCCULT BLOOD (FOB) TEST
December 19, 2012
K110889
IND ONE STEP HCG URINE PREGNANCY TEST (STRIP)
June 20, 2011