Form 483

Puracon GmbH Form 483, 2014-08-07

FDA issued a Form 483 to Puracon GmbH on 2014-08-07 with 5 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health5 observations

Puracon GmbH · Rosenheim, Germany · Issued August 7, 2014

Overview

  • 5 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.

7 Aug 2014
21 CFR 820.22

Quality audits - Lack of or inadequate procedures

Cited by Catherine J Laufmann

7 Aug 2014
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Catherine J Laufmann

7 Aug 2014
21 CFR 820.90(b)(1)

Procedures for product review,disposition lack of/inadequate

Cited by Catherine J Laufmann

7 Aug 2014
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Catherine J Laufmann

7 Aug 2014
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Catherine J Laufmann

Inspected site

PGPuracon GmbHRosenheim, Germany

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x
21 CFR 820.90(b)(1)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