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Procter & Gamble Manufacturing GmbH — FDA Facility Profile

FEI 3001903296

Procter & Gamble Manufacturing GmbH is an FDA-registered facility (FEI 3001903296) located in GROSS-GERAU Hesse, DE. Registered operations: ANALYSIS; LABEL; MANUFACTURE; PACK. RegDataLab tracks 2 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Mar 15, 2023: Voluntary Action Indicated (VAI)
Inspections on record
2 (2 VAI)
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
Import refusals
6

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
Mar 15, 2023Voluntary Action Indicated (VAI)No citations listed
Jul 24, 2015Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Procter & Gamble Manufacturing GmbH
Location
GROSS-GERAU Hesse (DE)
Registration Expires
Dec 31, 2027
Operations
ANALYSIS; LABEL; MANUFACTURE; PACK
Source
both

Import refusals

FDA data resources

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