Form 483

IKI Mfg Co., Inc Form 483, 2009-05-06

FDA issued a Form 483 to IKI Mfg Co., Inc on 2009-05-06 with 5 public-safe observations.

483· Form 483 issued5 observations

IKI Mfg Co., Inc · Edgerton, United States · Issued May 6, 2009

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 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.

6 May 2009
21 CFR 211.25(a)

GMP Training Frequency

Cited by Justin A Boyd, Charles Cote

6 May 2009
21 CFR 211.63

Equipment Design, Size and Location

Cited by Justin A Boyd, Charles Cote

6 May 2009
21 CFR 211.67(a)

Cleaning / Sanitizing / Maintenance

Cited by Justin A Boyd, Charles Cote

6 May 2009
21 CFR 211.67(b)

Written procedures not established/followed

Cited by Justin A Boyd, Charles Cote

6 May 2009
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Justin A Boyd, Charles Cote

Inspected site

IMIKI Mfg Co., IncEdgerton, United States

Inspection team

CCCharles Cote

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 211.25(a)Cited across public-safe Form 483 observations1x
21 CFR 211.63Cited across public-safe Form 483 observations1x
21 CFR 211.67(a)Cited across public-safe Form 483 observations1x
21 CFR 211.67(b)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 5 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