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RELITECH B.V. FDA Inspection Record

FEI 3014377913 · Inspections, Form 483s, warning letters and import refusals

RELITECH B.V. is an FDA-registered facility (FEI 3014377913) located in Nijkerk Gelderland, NL. RegDataLab tracks 1 FDA inspection at this facility.

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What FDA found at this site

Latest inspection
May 1, 2025: Voluntary Action Indicated (VAI)
Inspections on record
1 (1 VAI)
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
May 1, 2025Voluntary Action Indicated (VAI)Lack of or inadequate complaint procedures (21 CFR 820.198(a))

Facility details

Company
Relitech B.V.
Location
Nijkerk Gelderland (NL)
Source
device

FDA data resources

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