FDA-Inspected Site

Hospira, Inc.

32 FDA inspections are on record for Hospira, Inc. in Mcpherson, United States.

483· Form 483 issued

Mcpherson, United States · Last updated July 9, 2026

Overview

  • 32 FDA inspections are on record.
  • 17 inspections produced a Form 483.
  • The most recent recorded inspection date is 2026-03-10.

At a glance

Inspections

32

Form 483s

17

EIRs

16

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
2 Mar 2026 – 10 Mar 2026Human Drugs483On file
8 Jan 2025 – 17 Jan 2025Human Drugs483View 483 →
21 Mar 2024 – 27 Mar 2024BiologicsClean
26 Jun 2023 – 30 Jun 2023Human Drugs483On file
30 Aug 2021 – 3 Sep 2021BiologicsClean
9 Dec 2019 – 17 Jan 2020Human Drugs483View 483 →
23 Jul 2018 – 15 Aug 2018Human Drugs483On file
23 Jul 2018 – 8 Aug 2018Human Drugs483On file
12 Feb 2018 – 15 Feb 2018Human DrugsClean
16 Oct 2017 – 27 Oct 2017Human Drugs483On file
16 May 2016 – 8 Jun 2016Medical Devices & Rad HealthWLOn file
23 Mar 2015 – 3 Apr 2015Human Drugs483View 483 →

Observations on record

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

17 Jan 2025
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Chad W Rice, Jacob G Lutz, Monica E Murie, Eric D Bowles

17 Jan 2025
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by Chad W Rice, Jacob G Lutz, Monica E Murie, Eric D Bowles

17 Jan 2025
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Chad W Rice, Jacob G Lutz, Monica E Murie, Eric D Bowles

17 Jan 2020
21 CFR 211.100(b)

SOPs not followed / documented

Cited by Jazmine N Still, Simone E Pitts, Scott A Golladay

17 Jan 2020
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Jazmine N Still, Simone E Pitts, Scott A Golladay

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 211.192Cited across public-safe Form 483 observations4x
21 CFR 211.113(b)Cited across public-safe Form 483 observations3x
21 CFR 211.110(a)Cited across public-safe Form 483 observations2x
21 CFR 211.46(c)Cited across public-safe Form 483 observations2x
21 CFR 211.100(a)Cited across public-safe Form 483 observations1x
21 CFR 211.100(b)Cited across public-safe Form 483 observations1x
21 CFR 211.110(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)(4)Cited across public-safe Form 483 observations1x
21 CFR 211.165(d)Cited across public-safe Form 483 observations1x
21 CFR 211.184(b)Cited across public-safe Form 483 observations1x
21 CFR 211.186(b)(9)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x
21 CFR 211.80(a)Cited across public-safe Form 483 observations1x
21 CFR 211.84(d)(3)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Hospira, Inc.'s 17 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