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IOI Oleo GmbH FDA Inspection Record

FEI 3002807213 · Inspections, Form 483s, warning letters and import refusals

IOI Oleo GmbH is an FDA-registered facility (FEI 3002807213) located in Witten, DE. Registered operations: API MANUFACTURE. RegDataLab tracks 4 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Jul 25, 2024: Voluntary Action Indicated (VAI)
Inspections on record
4 (3 VAI, 1 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
Import refusals
2

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 25, 2024Voluntary Action Indicated (VAI)No citations listed
Jan 17, 2020Voluntary Action Indicated (VAI)No citations listed
Feb 27, 2015No Action Indicated (NAI)No citations listed
May 7, 2009Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
IOI OLEO GMBH
Location
Witten (DE)
Registration Expires
Dec 31, 2027
Operations
API MANUFACTURE
Source
decrs

Import refusals

FDA data resources

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