FDA-Inspected Site

MRP, LLC

13 FDA inspections are on record for MRP, LLC in Nashville, United States.

483· Form 483 issued

Nashville, United States · Last updated July 10, 2026

Overview

  • 13 FDA inspections are on record.
  • 8 inspections produced a Form 483.
  • The most recent recorded inspection date is 2022-10-18.

At a glance

Inspections

13

Form 483s

8

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
11 Oct 2022 – 18 Oct 2022Medical Devices & Rad Health483View 483 →
18 Feb 2020 – 27 Feb 2020Medical Devices & Rad Health483View 483 →
19 Apr 2016 – 28 Apr 2016Medical Devices & Rad Health483View 483 →
13 Jan 2015 – 23 Jan 2015Medical Devices & Rad Health483View 483 →
25 Feb 2013 – 7 Mar 2013Medical Devices & Rad Health483View 483 →
16 Nov 2012Not recordedClean
6 Oct 2010Not recorded483On file
15 Jan 2010Not recorded483On file
24 Oct 2008Not recorded483View 483 →
18 Mar 2008Not recordedClean
11 May 2006Not recordedClean
22 Jan 2004Not recordedClean

Observations on record

Form 483 observations cited at this site, most recent first.

18 Oct 2022
21 CFR 820.100(b)

Documentation

Cited by Mary A Millner, Jamie P Webb

18 Oct 2022
21 CFR 820.150

Lack of or inadequate procedures for storage.

Cited by Mary A Millner, Jamie P Webb

27 Feb 2020
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Mary A Millner

27 Feb 2020
21 CFR 820.250(a)

Statistical techniques - Lack of or inadequate procedures

Cited by Mary A Millner

27 Feb 2020
21 CFR 820.30(f)

Design verification - output does not meet input requirement

Cited by Mary A Millner

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations4x
21 CFR 820.100(b)Cited across public-safe Form 483 observations4x
21 CFR 820.70(c)Cited across public-safe Form 483 observations3x
21 CFR 820.75(b)Cited across public-safe Form 483 observations3x
21 CFR 820.80(c)Cited across public-safe Form 483 observations3x
21 CFR 820.75(c)Cited across public-safe Form 483 observations2x
21 CFR 820.80(a)Cited across public-safe Form 483 observations2x
21 CFR 803.17Cited across public-safe Form 483 observations1x
21 CFR 820.120(b)Cited across public-safe Form 483 observations1x
21 CFR 820.150Cited across public-safe Form 483 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.20Cited across public-safe Form 483 observations1x
21 CFR 820.20(a)Cited across public-safe Form 483 observations1x
21 CFR 820.20(b)Cited across public-safe Form 483 observations1x
21 CFR 820.20(b)(1)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.25(b)Cited across public-safe Form 483 observations1x
21 CFR 820.250(a)Cited across public-safe Form 483 observations1x
21 CFR 820.30(f)Cited across public-safe Form 483 observations1x
21 CFR 820.70(a)Cited across public-safe Form 483 observations1x
21 CFR 820.70(b)Cited across public-safe Form 483 observations1x
21 CFR 820.70(d)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind MRP, LLC's 8 Form 483s

Source PDFs, verbatim observations, and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat