Form 483

Teva Pharmaceuticals USA, Inc Form 483, 2010-03-01

FDA issued a Form 483 to Teva Pharmaceuticals USA, Inc on 2010-03-01 with 5 public-safe observations.

483· Form 483 issued5 observations

Teva Pharmaceuticals USA, Inc · Parsippany, United States · Issued March 1, 2010

Overview

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

1 Mar 2010
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Gayle S Lawson, Linda M Hoover

1 Mar 2010
21 CFR 211.198(a)

Adverse Drug Experience

Cited by Gayle S Lawson, Linda M Hoover

1 Mar 2010
21 CFR 211.198(a)

Complaint Handling Procedure

Cited by Gayle S Lawson, Linda M Hoover

1 Mar 2010
21 CFR 314.81(b)(1)(ii)

Failure to meet specifications

Cited by Gayle S Lawson, Linda M Hoover

1 Mar 2010
21 CFR 314.81(b)(2)(i)

Summary

Cited by Gayle S Lawson, Linda M Hoover

Inspected site

TPTeva Pharmaceuticals USA, IncParsippany, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.198(a)Cited across public-safe Form 483 observations2x
21 CFR 211.110(a)Cited across public-safe Form 483 observations1x
21 CFR 314.81(b)(1)(ii)Cited across public-safe Form 483 observations1x
21 CFR 314.81(b)(2)(i)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