FDA Inspection 1288376 — IRAY IMAGING LLC

IRAY IMAGING LLC — FEI 3030898585

The FDA completed an inspection of IRAY IMAGING LLC on Oct 24, 2025 in Solon, OH. 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). 4 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 24, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Solon, OH (United States)

Citations

IDCFRDescription
310221 CFR 820.30(h)Design transfer - Lack of or inadequate procedures
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.