Form 483

KEDPlasma LLC Form 483, 2012-12-05

FDA issued a Form 483 to KEDPlasma LLC on 2012-12-05 with 6 public-safe observations.

483· Form 483 issued6 observations

KEDPlasma LLC · Williamsville, United States · Issued December 5, 2012

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.

5 Dec 2012
21 CFR 600.10(b)

Personnel capabilities

Cited by Irina Gaberman

5 Dec 2012
21 CFR 606.65(e)

Following manufacturer's instructions

Cited by Irina Gaberman

5 Dec 2012
21 CFR 606.100(b)

Establish, maintain and follow manufacturing SOPs

Cited by Irina Gaberman

5 Dec 2012
21 CFR 606.100(c)

Record review prior to release

Cited by Irina Gaberman

5 Dec 2012
21 CFR 606.120(b)(2)

Destruction of obsolete labels

Cited by Irina Gaberman

Inspected site

KLKEDPlasma LLCWilliamsville, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 600.10(b)Cited across public-safe Form 483 observations1x
21 CFR 606.100(b)Cited across public-safe Form 483 observations1x
21 CFR 606.100(c)Cited across public-safe Form 483 observations1x
21 CFR 606.120(b)(2)Cited across public-safe Form 483 observations1x
21 CFR 606.160(a)(1)Cited across public-safe Form 483 observations1x
21 CFR 606.65(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