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Instrumed GmbH Dba Avalign German Specialty Instruments FDA Inspection Record

FEI 3007290840 · Inspections, Form 483s, warning letters and import refusals

Instrumed GmbH Dba Avalign German Specialty Instruments is an FDA-registered facility (FEI 3007290840) located in TUTTLINGEN Baden-Wurttemberg, DE. RegDataLab tracks 3 FDA inspections and 1 compliance action at this facility.

What FDA found at this site

Latest inspection
Oct 25, 2018: No Action Indicated (NAI)
Inspections on record
3 (1 OAI, 2 NAI)
Last OAI inspection
Aug 1, 2013
Warning letters
1 listed by FDA for this FEI, latest Mar 28, 2014
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
Oct 25, 2018No Action Indicated (NAI)No citations listed
Jan 29, 2015No Action Indicated (NAI)No citations listed
Aug 1, 2013Official Action Indicated (OAI)No citations listed

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Instrumed GmbH
Location
TUTTLINGEN Baden-Wurttemberg (DE)
Source
device

Compliance actions

Import refusals

FDA data resources

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