Form 483

Huvepharma, Inc. Form 483, 2019-04-23

FDA issued a Form 483 to Huvepharma, Inc. on 2019-04-23 with 5 public-safe observations.

483· Form 483 issuedAnimal Drugs & Feeds5 observations

Huvepharma, Inc. · Longmont, United States · Issued April 23, 2019

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.

23 Apr 2019
21 CFR 211.100(a)

Approval and review of procedures

Cited by Farhana Khan

23 Apr 2019
21 CFR 211.160(b)(1)

Sampling and testing procedures described

Cited by Farhana Khan

23 Apr 2019
21 CFR 211.22(a)

Contract drug products--lack of responsibility

Cited by Farhana Khan

23 Apr 2019
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Farhana Khan

23 Apr 2019
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Farhana Khan

Inspected site

HIHuvepharma, Inc.Longmont, 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 211.160(b)(1)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.22(a)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 5 observations

The source PDF and 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