Form 483

Michigan Instruments, Inc. Form 483, 2011-12-16

FDA issued a Form 483 to Michigan Instruments, Inc. on 2011-12-16 with 4 public-safe observations.

483· Form 483 issued4 observations

Michigan Instruments, Inc. · Grand Rapids, United States · Issued December 16, 2011

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

16 Dec 2011
21 CFR 820.75(a)

Documentation

Cited by Bleta Vuniqi, Martha Sullivan Myrick

16 Dec 2011
21 CFR 820.80(e)

Documentation

Cited by Bleta Vuniqi, Martha Sullivan Myrick

16 Dec 2011
21 CFR 820.90(a)

Nonconforming product control

Cited by Bleta Vuniqi, Martha Sullivan Myrick

16 Dec 2011
21 CFR 820.100(b)

Documentation

Cited by Bleta Vuniqi, Martha Sullivan Myrick

Inspected site

MIMichigan Instruments, Inc.Grand Rapids, United States

Inspection team

MSMartha Sullivan Myrick

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(b)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x
21 CFR 820.80(e)Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 observations

Every observation in full, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere