FDA Inspection 1181641 — MRP, LLC

MRP, LLC — FEI 1000151124

The FDA completed an inspection of MRP, LLC on October 18, 2022 in Nashville, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

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

Citations

IDCFRDescription
1471021 CFR 820.150Lack of or inadequate procedures for storage.
369621 CFR 820.100(b)Documentation