FDA Inspection 1191773 — Biedermann Motech, Inc.

Biedermann Motech, Inc. — FEI 3013248720

The FDA completed an inspection of Biedermann Motech, Inc. on November 23, 2022 in Miami, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 23, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Miami, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures