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ALS Scandinavia AB — FDA Facility Profile

FEI 3007165135

ALS Scandinavia AB is an FDA-registered facility (FEI 3007165135) located in Lulea, SE. Registered operations: ANALYSIS. RegDataLab tracks 5 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Oct 10, 2024: Voluntary Action Indicated (VAI)
Inspections on record
5 (3 VAI, 2 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

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
Oct 10, 2024Voluntary Action Indicated (VAI)No citations listed
Feb 9, 2022No Action Indicated (NAI)No citations listed
May 16, 2014Voluntary Action Indicated (VAI)No citations listed
May 31, 2011Voluntary Action Indicated (VAI)No citations listed
Nov 3, 2008No Action Indicated (NAI)No citations listed

Facility details

Company
ALS Scandinavia AB
Location
Lulea (SE)
Registration Expires
Dec 31, 2027
Operations
ANALYSIS
Source
decrs

FDA data resources

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