FDA Inspection 1155995 — Beckman Coulter, Inc.

Beckman Coulter, Inc. — FEI 3000203293

The FDA completed an inspection of Beckman Coulter, Inc. on October 28, 2021 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
October 28, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Miami, FL (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
73221 CFR 803.50(a)(2)Individual Report of Malfunction