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NOBILUS ENT ODDZIAL KUTNO — FDA Facility Profile

FEI 3008517755

NOBILUS ENT ODDZIAL KUTNO is an FDA-registered facility (FEI 3008517755) located in Poland (POL). Registered operations: ANALYSIS; API MANUFACTURE; LABEL. RegDataLab tracks 5 FDA inspections and 1 compliance action at this facility.

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What FDA found at this site

Latest inspection
May 9, 2024: Voluntary Action Indicated (VAI)
Inspections on record
5 (1 OAI, 2 VAI, 2 NAI)
Last OAI inspection
Sep 15, 2011
Warning letters
1 listed by FDA for this FEI, latest Mar 7, 2012

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
May 9, 2024Voluntary Action Indicated (VAI)No citations listed
Jul 11, 2019Voluntary Action Indicated (VAI)No citations listed
Sep 15, 2017No Action Indicated (NAI)No citations listed
Dec 18, 2014No Action Indicated (NAI)No citations listed
Sep 15, 2011Official Action Indicated (OAI)No citations listed

Facility details

Company
Nobilus Ent Oddzial Kutno
Location
Poland (POL)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; API MANUFACTURE; LABEL
Source
decrs

Compliance actions

FDA data resources

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