Form 483

Hillestad Pharmaceuticals USA, Inc. Form 483, 2011-05-12

FDA issued a Form 483 to Hillestad Pharmaceuticals USA, Inc. on 2011-05-12 with 4 public-safe observations.

483· Form 483 issued4 observations

Hillestad Pharmaceuticals USA, Inc. · Woodruff, United States · Issued May 12, 2011

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 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 May 2011
21 CFR 111.27(a)

Equipment - design - suitable

Cited by Justin A Boyd

12 May 2011
21 CFR 111.75(a)(2)(ii)(A)

Component - qualify supplier

Cited by Justin A Boyd

12 May 2011
21 CFR 111.255(b)

Batch record - complete

Cited by Justin A Boyd

12 May 2011
21 CFR 111.570(b)(2)(ii)(F)

Record - product complaint; findings

Cited by Justin A Boyd

Inspected site

HPHillestad Pharmaceuticals USA, Inc.Woodruff, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 111.255(b)Cited across public-safe Form 483 observations1x
21 CFR 111.27(a)Cited across public-safe Form 483 observations1x
21 CFR 111.570(b)(2)(ii)(F)Cited across public-safe Form 483 observations1x
21 CFR 111.75(a)(2)(ii)(A)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 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