FDA-Inspected Site

Huvepharma, Inc.

9 FDA inspections are on record for Huvepharma, Inc. in Longmont, United States.

483· Form 483 issued

Longmont, United States · Last updated July 9, 2026

Overview

  • 9 FDA inspections are on record.
  • 7 inspections produced a Form 483.
  • The most recent recorded inspection date is 2019-04-23.

At a glance

Inspections

9

Form 483s

7

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
16 Apr 2019 – 23 Apr 2019Animal Drugs & Feeds483View 483 →
7 Jul 2017 – 14 Jul 2017Animal Drugs & Feeds483View 483 →
14 Nov 2016 – 23 Nov 2016Animal Drugs & Feeds483View 483 →
30 Nov 2015 – 4 Dec 2015Animal Drugs & Feeds483View 483 →
3 Dec 2013 – 12 Dec 2013Animal Drugs & Feeds483On file
21 Feb 2012Not recorded483View 483 →
9 Jun 2010Not recordedClean
25 Jul 2008Not recorded483On file
1 Feb 2001Not recordedClean

Observations on record

Form 483 observations cited at this site, most recent first.

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

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 211.68(b)Cited across public-safe Form 483 observations6x
21 CFR 211.192Cited across public-safe Form 483 observations4x
21 CFR 211.100(b)Cited across public-safe Form 483 observations3x
21 CFR 211.166(a)Cited across public-safe Form 483 observations3x
21 CFR 211.182Cited across public-safe Form 483 observations3x
21 CFR 211.160(a)Cited across public-safe Form 483 observations2x
21 CFR 211.180(e)(1)Cited across public-safe Form 483 observations2x
21 CFR 211.194(a)(4)Cited across public-safe Form 483 observations2x
21 CFR 211.22(d)Cited across public-safe Form 483 observations2x
21 CFR 211.100(a)Cited across public-safe Form 483 observations1x
21 CFR 211.110(a)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)(1)Cited across public-safe Form 483 observations1x
21 CFR 211.22(a)Cited across public-safe Form 483 observations1x
21 CFR 211.22(b)Cited across public-safe Form 483 observations1x
21 CFR 211.56(b)Cited across public-safe Form 483 observations1x
21 CFR 211.68(a)Cited across public-safe Form 483 observations1x
21 CFR 226.1Cited across public-safe Form 483 observations1x
21 CFR 226.30Cited across public-safe Form 483 observations1x
21 CFR 226.40(e)Cited across public-safe Form 483 observations1x
21 CFR 314.81(b)(1)(ii)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Huvepharma, Inc.'s 7 Form 483s

Source PDFs, verbatim observations, and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat