Laboratoires Bodycad, Inc.

FDA Regulatory Profile

Laboratoires Bodycad, 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-0244-2022, Class II) was initiated on July 2, 2021.

Summary

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

Recent Recalls

NumberClassProductDate
Z-0244-2022Class IITorque Limiting Adaptor, AO Connect, 4 N-m, part #027-203, reusable, a component of the Bodycad FineJuly 2, 2021