FDA Inspection 1254718 — Exotoe LLC

Exotoe LLC — FEI 3015200653

The FDA completed an inspection of Exotoe LLC on Nov 21, 2024 in Charlotte, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 21, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Charlotte, NC (United States)

Citations

IDCFRDescription
310221 CFR 820.30(h)Design transfer - Lack of or inadequate procedures
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
315921 CFR 820.184DHR content
319321 CFR 820.30(g)Design validation - simulated testing