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FDA Inspection 700456 — MRP, LLC

MRP, LLC — FEI 1000151124

The FDA completed an inspection of MRP, LLC on October 6, 2010 in Nashville, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 6, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Nashville, TN (United States)

Facility

Other inspections at this facility

  • 1181641 (VAI Tue Oct 18 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1119238 (VAI Thu Feb 27 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 968508 (OAI Thu Apr 28 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 909773 (NAI Fri Jan 23 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 823632 (VAI Thu Mar 07 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources