Form 483

Huvepharma, Inc. Form 483, 2018-05-22

FDA issued a Form 483 to Huvepharma, Inc. on 2018-05-22 with 6 public-safe observations.

483· Form 483 issuedAnimal Drugs & Feeds6 observations

Huvepharma, Inc. · Saint Louis, United States · Issued May 22, 2018

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.

22 May 2018
21 CFR 211.25(a)

Training , Education , Experience overall

Cited by Kellia N Hicks

22 May 2018
21 CFR 211.68(b)

Computer control of master formula records

Cited by Kellia N Hicks

22 May 2018
21 CFR 211.160(a)

Following/documenting laboratory controls

Cited by Kellia N Hicks

22 May 2018
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Kellia N Hicks

22 May 2018
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Kellia N Hicks

Inspected site

HIHuvepharma, Inc.Saint Louis, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.160(a)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x
21 CFR 211.25(a)Cited across public-safe Form 483 observations1x
21 CFR 211.68(b)Cited across public-safe Form 483 observations1x
21 CFR 211.80(b)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 6 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