FDA Inspection 1181689 — iMed Technology, Inc

iMed Technology, Inc — FEI 3003813437

The FDA completed an inspection of iMed Technology, Inc on Oct 18, 2022 in Mckinney, TX. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 18, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Mckinney, TX (United States)

Citations

IDCFRDescription
232821 CFR 820.22Quality audits - auditor independence

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