Form 483

WHPM Inc. Form 483, 2022-11-18

FDA issued a Form 483 to WHPM Inc. on 2022-11-18 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

WHPM Inc. · Irwindale, United States · Issued November 18, 2022

Overview

  • 6 public-safe observations are available for this inspection.
  • 3 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.

18 Nov 2022
21 CFR 803.17(b)(1)

Info evaluated to determine if event was reportable

Cited by Marlo-Ian M Alintanahin

18 Nov 2022
21 CFR 803.17(b)(1)

Info evaluated to determine if event was reportable

Cited by Marlo-Ian M Alintanahin

18 Nov 2022
21 CFR 820.160(a)

Lack of or inadequate procedures for distribution

Cited by Marlo-Ian M Alintanahin

18 Nov 2022
21 CFR 820.160(a)

Lack of or inadequate procedures for distribution

Cited by Marlo-Ian M Alintanahin

18 Nov 2022
21 CFR 820.50(a)(3)

Acceptable supplier records, inadequate records

Cited by Marlo-Ian M Alintanahin

Inspected site

WIWHPM Inc.Irwindale, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17(b)(1)Cited across public-safe Form 483 observations2x
21 CFR 820.160(a)Cited across public-safe Form 483 observations2x
21 CFR 820.50(a)(3)Cited across public-safe Form 483 observations2x

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 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