FDA Inspection 1151858 — Miami Device Solutions, LLC.

Miami Device Solutions, LLC. — FEI 3009222247

The FDA completed an inspection of Miami Device Solutions, LLC. on September 16, 2021 in Miami, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 16, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Miami, FL (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation