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Intertek — Royston

Royston, United Kingdom · Testing lab

This is a record of what regulators published, not a rating.

Site facts

Company
Intertek
Name(s) in FDA data
Melbourn Scientific Limited (d.b.a. Intertek Melbourn)
FEI number(s)
3002807539 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Royston, United Kingdom
Records matched
7 FDA inspections
Most recent FDA inspection in dataset
30 Jun 2023 — VAI

Capabilities (from the company's website)

  • Analytical testing
    …y formats. Furthermore, dedicated laboratory spaces will be established for comprehensive analytical testing, particle engineering, device selection, characterisation and performance testing, reinfo…

Taken from the company's web page for this site. Source: https://www.intertek.com/news/2025/intertek-expands-pharmaceutical-services-capacity-with-acquisition-of-new-facility-in-melbourn-cambridge/, checked 16 Oct 2026. Quoted text shows the wording each tag is based on.

Regulatory timeline

Newest first. Each entry links to the published source. Inspection classifications: NAI = no action indicated, VAI = voluntary action indicated, OAI = official action indicated (FDA definitions). Posted 483 citations are FDA's short summaries, not the full Form 483.

  1. 30 Jun 2023
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Drugs. Project area(s): Bioresearch Monitoring.

    Source: FDA Data Dashboard – Inspections (FEI 3002807539, inspection ID 1220505)

  2. 16 Jun 2022
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002807539, inspection ID 1208592)

  3. 29 Nov 2019
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Drugs. Project area(s): Bioresearch Monitoring.

    Source: FDA Data Dashboard – Inspections (FEI 3002807539, inspection ID 1116933)

  4. 29 Nov 2019
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Drugs. Project area(s): Bioresearch Monitoring.

    Source: FDA Data Dashboard – Inspections (FEI 3002807539, inspection ID 1115204)

  5. 01 Nov 2016
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002807539, inspection ID 989768)

  6. 23 Jul 2012
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002807539, inspection ID 794873)

  7. 11 Aug 2009
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002807539, inspection ID 635302)

This is a record of what regulators published, not a rating. Absence of a record here does not mean no record exists; see methodology for what we check and how records are matched.