Form 483

QuVa Pharma, Inc. Form 483, 2019-05-31

FDA issued a Form 483 to QuVa Pharma, Inc. on 2019-05-31 with 6 public-safe observations.

483· Form 483 issuedHuman Drugs6 observations

QuVa Pharma, Inc. · Bloomsbury, United States · Issued May 31, 2019

Overview

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

31 May 2019
21 CFR 211.113(b)

Validation lacking for sterile drug products

Cited by Guerlain Ulysse

31 May 2019
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Guerlain Ulysse

31 May 2019
21 CFR 211.198(b)(2)

Written record of complaint to include findings, follow-up

Cited by Guerlain Ulysse

31 May 2019
21 CFR 211.22(c)

Approve or reject procedures or specs

Cited by Guerlain Ulysse

31 May 2019
21 CFR 211.42(c)(10)(iv)

Environmental Monitoring System

Cited by Guerlain Ulysse

Inspected site

QPQuVa Pharma, Inc.Bloomsbury, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.113(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 211.198(b)(2)Cited across public-safe Form 483 observations1x
21 CFR 211.22(c)Cited across public-safe Form 483 observations1x
21 CFR 211.42(c)(10)(iv)Cited across public-safe Form 483 observations1x
21 CFR 211.84(d)(2)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 6 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