Form 483

King Bio Inc Form 483, 2011-08-10

FDA issued a Form 483 to King Bio Inc on 2011-08-10 with 6 public-safe observations.

483· Form 483 issued6 observations

King Bio Inc · Asheville, United States · Issued August 10, 2011

Overview

  • 6 public-safe observations are available for this inspection.
  • 6 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.

10 Aug 2011
21 CFR 211.25(a)

Training , Education , Experience overall

Cited by Edward Deberry

10 Aug 2011
21 CFR 211.84(e)

Rejecting When Specifications Not Met

Cited by Edward Deberry

10 Aug 2011
21 CFR 211.165(b)

Microbiological testing

Cited by Edward Deberry

10 Aug 2011
21 CFR 211.166(a)

Written program not followed

Cited by Edward Deberry

10 Aug 2011
21 CFR 211.186(b)(9)

Manufacturing Instructions and Specifications

Cited by Edward Deberry

Inspected site

KBKing Bio IncAsheville, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.165(b)Cited across public-safe Form 483 observations1x
21 CFR 211.166(a)Cited across public-safe Form 483 observations1x
21 CFR 211.186(b)(9)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.25(a)Cited across public-safe Form 483 observations1x
21 CFR 211.84(e)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 6 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