The Procter & Gamble Manufacturing Company FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

The Procter & Gamble Manufacturing Company has 0 FDA recalls, 30 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "The Procter & Gamble Manufacturing Company" is on file.

What these totals cover: FDA records filed under the name "The Procter & Gamble Manufacturing Company" and its spelling variant "Procter And Gamble Manufacturing".

Latest inspection
Jun 9, 2026 · OAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections30Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

The Procter & Gamble Manufacturing Company's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

The Procter & Gamble Manufacturing Company: FDA inspections per year 2017: 2 inspections220172018: 1 inspections120182019: 0 inspections020192020: 1 inspections120202021: 1 inspections120212022: 2 inspections220222023: 2 inspections220232024: 2 inspections220242025: 0 inspections020252026: 1 inspections12026
YearInspectionsOAIWarning lettersRecall recordsClass I
202611000
202500000
202420000
202320000
202220000
202110000
202010000
201900000
201810000
201720000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA inspections

30 inspections from Aug 20, 2009 to Jun 9, 2026. Showing the 20 most recent. View all 30 inspections

DateSiteProductClassificationFEI
Jun 9, 2026Greensboro, NCDrugsOfficial Action Indicated (OAI)1017175
Sep 27, 2024Iowa City, IADrugsNo Action Indicated (NAI)1913771
Sep 11, 2024Inwood, WVDrugsVoluntary Action Indicated (VAI)1925189
Mar 15, 2023Gros-Gerau, GermanyDrugsVoluntary Action Indicated (VAI)3001903296
Mar 10, 2023Greensboro, NCDrugsVoluntary Action Indicated (VAI)1017175
Jun 3, 2022Phoenix, AZDrugsNo Action Indicated (NAI)2021299
Feb 18, 2022Browns Summit, NCDrugsVoluntary Action Indicated (VAI)1033800
Jul 12, 2021West Branch, IAFood/CosmeticsNo Action Indicated (NAI)3004274728
Feb 26, 2020Phoenix, AZFood/CosmeticsNo Action Indicated (NAI)2021299
Jan 5, 2018West Branch, IAFood/CosmeticsNo Action Indicated (NAI)3004274728
Nov 17, 2017Greensboro, NCDrugsVoluntary Action Indicated (VAI)1017175
Mar 10, 2017Browns Summit, NCDrugsVoluntary Action Indicated (VAI)1033800
Aug 15, 2016Phoenix, AZDrugsNo Action Indicated (NAI)2021299
May 27, 2016Inwood, WVDrugsNo Action Indicated (NAI)1925189
May 6, 2016Greensboro, NCDrugsNo Action Indicated (NAI)1017175
Sep 21, 2015Iowa City, IADrugsNo Action Indicated (NAI)1913771
Jul 24, 2015Gros-Gerau, GermanyDrugsVoluntary Action Indicated (VAI)3001903296
Jul 30, 2013West Branch, IAFood/CosmeticsNo Action Indicated (NAI)3004274728
Jul 18, 2013Greensboro, NCDrugsVoluntary Action Indicated (VAI)1017175
Jul 12, 2012Iowa City, IADrugsNo Action Indicated (NAI)1913771
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

7 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 1017175Greensboro, NC7Jun 9, 2026
FEI 1913771Iowa City, IA5Sep 27, 2024
FEI 1925189Inwood, WV2Sep 11, 2024
FEI 3001903296Gros-Gerau, Germany2Mar 15, 2023
FEI 2021299Phoenix, AZ7Jun 3, 2022
FEI 1033800Browns Summit, NC4Feb 18, 2022
FEI 3004274728West Branch, IA3Jul 12, 2021

The Procter & Gamble Manufacturing Company and the FDA: common questions

Has The Procter & Gamble Manufacturing Company received an FDA warning letter?

No FDA warning letter addressed to the name "The Procter & Gamble Manufacturing Company" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has The Procter & Gamble Manufacturing Company received an FDA Form 483?

FDA has not published a Form 483 for "The Procter & Gamble Manufacturing Company" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect The Procter & Gamble Manufacturing Company?

The most recent FDA inspection on file ended Jun 9, 2026 at Greensboro, NC and was classified OAI. FDA has 30 inspections of The Procter & Gamble Manufacturing Company on file, 1 of them classified OAI (official action indicated).

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