Form 483

Mani, Inc. - Kiyohara Facility Form 483, 2010-10-07

FDA issued a Form 483 to Mani, Inc. - Kiyohara Facility on 2010-10-07 with 5 public-safe observations.

483· Form 483 issued5 observations

Mani, Inc. - Kiyohara Facility · Utsunomiya, Japan · Issued October 7, 2010

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

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

7 Oct 2010
21 CFR 820.22

Quality audits - Lack of or inadequate procedures

Cited by Frank J Marciniak

7 Oct 2010
21 CFR 820.25(b)

Training records

Cited by Frank J Marciniak

7 Oct 2010
21 CFR 820.100(b)

Documentation

Cited by Frank J Marciniak

7 Oct 2010
21 CFR 820.198(a)

Complaints

Cited by Frank J Marciniak

7 Oct 2010
21 CFR 820.250(b)

Sampling plans

Cited by Frank J Marciniak

Inspected site

Inspection team

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 820.198(a)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(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