Form 483

Nice-Pak Products, Inc. Form 483, 2010-02-10

FDA issued a Form 483 to Nice-Pak Products, Inc. on 2010-02-10 with 6 public-safe observations.

483· Form 483 issued6 observations

Nice-Pak Products, Inc. · Mooresville, United States · Issued February 10, 2010

Overview

  • 6 public-safe observations are available for this inspection.
  • 6 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.

10 Feb 2010
21 CFR 211.25(a)

GMP Training Frequency

Cited by Robert M Barbosa, Daniel J Gorski

10 Feb 2010
21 CFR 211.68(b)

input/output verification

Cited by Robert M Barbosa, Daniel J Gorski

10 Feb 2010
21 CFR 211.100(a)

Absence of Written Procedures

Cited by Robert M Barbosa, Daniel J Gorski

10 Feb 2010
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Robert M Barbosa, Daniel J Gorski

10 Feb 2010
21 CFR 211.160(a)

Following/documenting laboratory controls

Cited by Robert M Barbosa, Daniel J Gorski

Inspected site

NPNice-Pak Products, Inc.Mooresville, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.100(a)Cited across public-safe Form 483 observations1x
21 CFR 211.100(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(a)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.25(a)Cited across public-safe Form 483 observations1x
21 CFR 211.68(b)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