FDA Inspection 1116281 — Macbrud Corporation

Macbrud Corporation — FEI 1052243

The FDA completed an inspection of Macbrud Corporation on January 23, 2020 in Miami, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 8 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 23, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Miami, FL (United States)

Citations

IDCFRDescription
1471621 CFR 820.30(f)Design verification - output does not meet input requirement
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
255721 CFR 820.30(c)Design input - documentation
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
319121 CFR 820.30(g)Design validation - production units
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures