Form 483

Vericel Corporation Form 483, 2009-08-21

FDA issued a Form 483 to Vericel Corporation on 2009-08-21 with 7 public-safe observations.

483· Form 483 issued7 observations

Vericel Corporation · Cambridge, United States · Issued August 21, 2009

Overview

  • 7 public-safe observations are available for this inspection.
  • 7 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.

21 Aug 2009
21 CFR 211.68(a)

Calibration/Inspection/Checking not done

Cited by Omotunde O Osunsanmi

21 Aug 2009
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Omotunde O Osunsanmi

21 Aug 2009
21 CFR 211.110(b)

In-process materials specifications testing

Cited by Omotunde O Osunsanmi

21 Aug 2009
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by Omotunde O Osunsanmi

21 Aug 2009
21 CFR 211.192

Written record of investigation incomplete

Cited by Omotunde O Osunsanmi

Inspected site

VCVericel CorporationCambridge, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.110(a)Cited across public-safe Form 483 observations1x
21 CFR 211.110(b)Cited across public-safe Form 483 observations1x
21 CFR 211.113(b)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.68(a)Cited across public-safe Form 483 observations1x
21 CFR 600.14(c)Cited across public-safe Form 483 observations1x
21 CFR 600.80(c)(1)(i)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 7 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