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The Procter & Gamble Manufacturing Company FDA Inspection Record

FEI 3004274728 · Inspections, Form 483s, warning letters and import refusals

The Procter & Gamble Manufacturing Company is an FDA-registered facility (FEI 3004274728) located in West Branch, IA, US. Registered operations: LABEL. RegDataLab tracks 3 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Jul 12, 2021: No Action Indicated (NAI)
Inspections on record
3 (3 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Jul 12, 2021No Action Indicated (NAI)No citations listed
Jan 5, 2018No Action Indicated (NAI)No citations listed
Jul 30, 2013No Action Indicated (NAI)No citations listed

Facility details

Company
The Procter & Gamble Manufacturing Company
Location
West Branch, IA (US)
Registration Expires
Dec 31, 2027
Operations
LABEL
Source
decrs

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.