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SANUM-Kehlbeck GmbH & Co. KG FDA Inspection Record

FEI 3002128313 · Inspections, Form 483s, warning letters and import refusals

SANUM-Kehlbeck GmbH & Co. KG is an FDA-inspected facility (FEI 3002128313) located in Hoya, DE. RegDataLab tracks 1 FDA inspection and 1 compliance action at this facility.

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What FDA found at this site

Latest inspection
Mar 26, 2013: Official Action Indicated (OAI)
Inspections on record
1 (1 OAI)
Last OAI inspection
Mar 26, 2013
Warning letters
1 listed by FDA for this FEI, latest Apr 11, 2014
Import refusals
10 or more

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 26, 2013Official Action Indicated (OAI)No citations listed

Facility details

Company
SANUM-Kehlbeck GmbH & Co. KG
Location
Hoya (DE)
Source
inspections

Compliance actions

Import refusals

FDA data resources

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