Form 483

DMD Pharmaceuticals Division of Dickey Consumer Products Inc Form 483, 2016-04-08

FDA issued a Form 483 to DMD Pharmaceuticals Division of Dickey Consumer Products Inc on 2016-04-08 with 5 public-safe observations.

483· Form 483 issuedFoods & Cosmetics5 observations

DMD Pharmaceuticals Division of Dickey Consumer Products Inc · Noblesville, United States · Issued April 8, 2016

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.

8 Apr 2016
21 CFR 111.105

Quality control - packaged, labeled

Cited by Linda S Jozefiak

8 Apr 2016
21 CFR 111.12(c)

Personnel - education, training, experience

Cited by Linda S Jozefiak

8 Apr 2016
21 CFR 111.140(b)(2)(ii)

Signature; review, approval, rejection; reprocessing

Cited by Linda S Jozefiak

8 Apr 2016
21 CFR 111.430(b)

Records - packaging, labeling operations

Cited by Linda S Jozefiak

8 Apr 2016
21 CFR 111.75(c)(3)

Specifications met identity,purity, strength, comp; basis

Cited by Linda S Jozefiak

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 111.105Cited across public-safe Form 483 observations1x
21 CFR 111.12(c)Cited across public-safe Form 483 observations1x
21 CFR 111.140(b)(2)(ii)Cited across public-safe Form 483 observations1x
21 CFR 111.430(b)Cited across public-safe Form 483 observations1x
21 CFR 111.75(c)(3)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