Form 483

Blairex Laboratories, Inc Form 483, 2013-12-12

FDA issued a Form 483 to Blairex Laboratories, Inc on 2013-12-12 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Blairex Laboratories, Inc · Columbus, United States · Issued December 12, 2013

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 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.

12 Dec 2013
21 CFR 211.68(a)

Calibration/Inspection/Checking not done

Cited by Robert M Barbosa

12 Dec 2013
21 CFR 211.142

Written warehousing procedures established/followed

Cited by Robert M Barbosa

12 Dec 2013
21 CFR 211.180(e)(2)

Items to cover on annual reviews

Cited by Robert M Barbosa

12 Dec 2013
21 CFR 211.198(a)

Complaint Handling Procedure

Cited by Robert M Barbosa

Inspected site

BLBlairex Laboratories, IncColumbus, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.142Cited across public-safe Form 483 observations1x
21 CFR 211.180(e)(2)Cited across public-safe Form 483 observations1x
21 CFR 211.198(a)Cited across public-safe Form 483 observations1x
21 CFR 211.68(a)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 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