IMMUNDIAGNOSTIK, Inc

FDA Regulatory Profile

IMMUNDIAGNOSTIK, Inc 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-1603-2023, Class II) was initiated on March 27, 2023.

Summary

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

Recent Recalls

NumberClassProductDate
Z-1603-2023Class IIImmundiagnostik IDK Lactoferrin ELISA- In vitro enzyme immunoassay intended for the determination ofMarch 27, 2023