Form 483

PureTek Corporation Form 483, 2010-07-16

FDA issued a Form 483 to PureTek Corporation on 2010-07-16 with 3 public-safe observations.

483· Form 483 issued3 observations

PureTek Corporation · San Fernando, United States · Issued July 16, 2010

Overview

  • 3 public-safe observations are available for this inspection.
  • 2 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.

16 Jul 2010
21 CFR 211.198(a)

Adverse Drug Experience

Cited by Richmond K Yip, S. L Brown

16 Jul 2010
21 CFR 211.198(a)

Complaint Handling Procedure

Cited by Richmond K Yip, S. L Brown

16 Jul 2010
21 CFR 211.198(b)

Records maintained for 1 year (except certain OTC drugs)

Cited by Richmond K Yip, S. L Brown

Inspected site

PCPureTek CorporationSan Fernando, United States

Inspection team

SLS. L Brown

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 211.198(b)Cited across public-safe Form 483 observations1x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 3 observations

The source PDF and 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