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MOOR INSTRUMENTS LTD. FDA Inspection Record

FEI 1000279065 · Inspections, Form 483s, warning letters and import refusals

MOOR INSTRUMENTS LTD. is an FDA-registered facility (FEI 1000279065) located in AXMINSTER Devon, GB. RegDataLab tracks 5 FDA inspections and 2 compliance actions at this facility.

What FDA found at this site

Latest inspection
Oct 27, 2022: No Action Indicated (NAI)
Inspections on record
5 (2 OAI, 2 VAI, 1 NAI)
Last OAI inspection
Aug 21, 2014
Warning letters
2 listed by FDA for this FEI, latest Dec 18, 2014
Import refusals
2

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 27, 2022No Action Indicated (NAI)No citations listed
Nov 7, 2019Voluntary Action Indicated (VAI)Product rework procedures, Lack of or inadequate procedures (21 CFR 820.90(b)(2))
Evaluation of suppliers, contractors, etc., requirements (21 CFR 820.50(a))
May 5, 2017Voluntary Action Indicated (VAI)Investigation of device failures (21 CFR 820.198(c))
Documentation (21 CFR 820.100(b))
Aug 21, 2014Official Action Indicated (OAI)No citations listed
May 6, 2011Official Action Indicated (OAI)Training - Lack of or inadequate procedures (21 CFR 820.25(b))
Design review - Lack of or inadequate procedures (21 CFR 820.30(e))
Lack of or inadequate procedures (21 CFR 820.100(a))
Complaints (21 CFR 820.198(a))
and 3 more

FDA record score

3 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 15, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

6 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAINov 7, 20196 x 0.251.5
Inspection classified VAIMay 5, 20176 x 0.251.5
Warning letter on FDA's dashboard, which does not show close-outsDec 18, 201410 years or older, so it adds no points0
Inspection classified OAIAug 21, 201410 years or older, so it adds no points0
Warning letter on FDA's dashboard, which does not show close-outsSep 6, 201110 years or older, so it adds no points0
Inspection classified OAIMay 6, 201110 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 15, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 15, 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 15, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 15, 2026Newest record Nov 5, 2026Current

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Facility details

Company
Moor Instruments Ltd
Location
AXMINSTER Devon (GB)
Source
device

Compliance actions

Import refusals

FDA data resources

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