Form 483

Biolitec, Inc. Form 483, 2010-02-23

FDA issued a Form 483 to Biolitec, Inc. on 2010-02-23 with 5 public-safe observations.

483· Form 483 issued5 observations

Biolitec, Inc. · E Longmeadow, United States · Issued February 23, 2010

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.

23 Feb 2010
21 CFR 820.72(a)

Calibration, Inspection, etc. Procedures Lack of or Inadequ

Cited by Emir Galevi, Brenda P King

23 Feb 2010
21 CFR 820.80(d)

Lack of or inadequate final acceptance procedures

Cited by Emir Galevi, Brenda P King

23 Feb 2010
21 CFR 820.90(a)

Specific non-conforming product procedures

Cited by Emir Galevi, Brenda P King

23 Feb 2010
21 CFR 1002.11

Failure to submit

Cited by Emir Galevi, Brenda P King

23 Feb 2010
21 CFR 1002.13

Lack of required elements

Cited by Emir Galevi, Brenda P King

Inspected site

BIBiolitec, Inc.E Longmeadow, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 1002.11Cited across public-safe Form 483 observations1x
21 CFR 1002.13Cited across public-safe Form 483 observations1x
21 CFR 820.72(a)Cited across public-safe Form 483 observations1x
21 CFR 820.80(d)Cited across public-safe Form 483 observations1x
21 CFR 820.90(a)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