Form 483

QuVa Pharma, Inc. Form 483, 2018-04-20

FDA issued a Form 483 to QuVa Pharma, Inc. on 2018-04-20 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

QuVa Pharma, Inc. · Temple, United States · Issued April 20, 2018

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.

20 Apr 2018
21 CFR 211.100(a)

Absence of Written Procedures

Cited by Scott T Ballard

20 Apr 2018
21 CFR 211.198(b)(2)

Written record of complaint to include findings, follow-up

Cited by Scott T Ballard

20 Apr 2018
21 CFR 211.22(a)

Authority lacking to review records, investigate errors

Cited by Scott T Ballard

20 Apr 2018
21 CFR 211.42(c)(10)

Aseptic Processing Area

Cited by Scott T Ballard

Inspected site

QPQuVa Pharma, Inc.Temple, 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 211.198(b)(2)Cited across public-safe Form 483 observations1x
21 CFR 211.22(a)Cited across public-safe Form 483 observations1x
21 CFR 211.42(c)(10)Cited across public-safe Form 483 observations1x

Source document

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Form 483 source document

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Full 483 report

Get the verbatim text of all 4 observations

The source PDF, 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