Form 483

The Procter & Gamble Manufacturing Company Form 483, 2026-06-09

FDA issued a Form 483 to The Procter & Gamble Manufacturing Company on 2026-06-09 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

The Procter & Gamble Manufacturing Company · Greensboro, United States · Issued June 9, 2026

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

9 Jun 2026
21 CFR 211.115(a)

Reprocessing procedures lack steps to be taken

Cited by Santos E Camara, Saundrea A Munroe

9 Jun 2026
21 CFR 211.166(a)

Written program not followed

Cited by Santos E Camara, Saundrea A Munroe

9 Jun 2026
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Santos E Camara, Saundrea A Munroe

9 Jun 2026
21 CFR 211.194(a)(1)

Description and Identification of Samples

Cited by Santos E Camara, Saundrea A Munroe

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.115(a)Cited across public-safe Form 483 observations1x
21 CFR 211.166(a)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.194(a)(1)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 observations

The full inspection record, as Atlas holds it, 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