FDA Inspection 1210642 — BALT USA, LLC

BALT USA, LLC — FEI 3014162263

The FDA completed an inspection of BALT USA, LLC on July 21, 2023 in Irvine, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 21, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)

Citations

IDCFRDescription
326621 CFR 820.86Acceptance status
369621 CFR 820.100(b)Documentation
73221 CFR 803.50(a)(2)Individual Report of Malfunction