Form 483

Patheon Puerto Rico, Inc. Form 483, 2013-06-12

FDA issued a Form 483 to Patheon Puerto Rico, Inc. on 2013-06-12 with 6 public-safe observations.

483· Form 483 issuedHuman Drugs6 observations

Patheon Puerto Rico, Inc. · Manati, United States · Issued June 12, 2013

Overview

  • 6 public-safe observations are available for this inspection.
  • 5 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 Jun 2013
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Libia M Lugo

12 Jun 2013
21 CFR 211.100(a)

Absence of Written Procedures

Cited by Libia M Lugo

12 Jun 2013
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Libia M Lugo

12 Jun 2013
21 CFR 211.166(a)

Results not used for expiration dates, storage cond.

Cited by Libia M Lugo

12 Jun 2013
21 CFR 211.192

Extent of discrepancy, failure investigations

Cited by Libia M Lugo

Inspected site

PPPatheon Puerto Rico, Inc.Manati, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.192Cited across public-safe Form 483 observations2x
21 CFR 211.100(a)Cited across public-safe Form 483 observations1x
21 CFR 211.110(a)Cited across public-safe Form 483 observations1x
21 CFR 211.166(a)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)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