Form 483

Octapharma Plasma, Inc. Form 483, 2018-05-24

FDA issued a Form 483 to Octapharma Plasma, Inc. on 2018-05-24 with 3 public-safe observations.

483· Form 483 issuedBiologics3 observations

Octapharma Plasma, Inc. · Fort Worth, United States · Issued May 24, 2018

Overview

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

24 May 2018
21 CFR 606.100(b)

Establish, maintain and follow manufacturing SOPs

Cited by Decarlos A Gomez

24 May 2018
21 CFR 606.40(a)(1)

Provide space for examination

Cited by Decarlos A Gomez

24 May 2018
21 CFR 640.64(e)

Prevention of contamination

Cited by Decarlos A Gomez

Inspected site

OPOctapharma Plasma, Inc.Fort Worth, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 606.100(b)Cited across public-safe Form 483 observations1x
21 CFR 606.40(a)(1)Cited across public-safe Form 483 observations1x
21 CFR 640.64(e)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 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