FDA Inspection 1268194 — Sunshine USA, LLC

Sunshine USA, LLC — FEI 3009973354

The FDA completed an inspection of Sunshine USA, LLC on Apr 28, 2025 in Johnson City, TN. 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
Apr 28, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Johnson City, TN (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
323321 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ

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