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FUJIFILM Diosynth Biotechnologies UK Ltd FDA Inspection Record

FEI 3007182567 · Inspections, Form 483s, warning letters and import refusals

FUJIFILM Diosynth Biotechnologies UK Ltd is an FDA-registered facility (FEI 3007182567) located in Billingham, GB. Registered operations: ANALYSIS; API MANUFACTURE. RegDataLab tracks 6 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Mar 17, 2023: Voluntary Action Indicated (VAI)
Inspections on record
6 (6 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
Import refusals
4

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
Mar 17, 2023Voluntary Action Indicated (VAI)No citations listed
Mar 25, 2021Voluntary Action Indicated (VAI)No citations listed
Nov 16, 2018Voluntary Action Indicated (VAI)No citations listed
Jul 11, 2014Voluntary Action Indicated (VAI)Approve or reject procedures or specs (21 CFR 211.22(c))
Training--operations, GMPs, written procedures (21 CFR 211.25(a))
Cleaning / Sanitizing / Maintenance (21 CFR 211.67(a))
Control procedures to monitor and validate performance (21 CFR 211.110(a))
and 1 more
Jun 20, 2012Voluntary Action Indicated (VAI)No citations listed
Jan 9, 2009Voluntary Action Indicated (VAI)No citations listed

FDA record score

7 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 VAIMar 17, 20236 x 0.63.6
Inspection classified VAIMar 25, 20216 x 0.251.5
Inspection classified VAINov 16, 20186 x 0.251.5
Inspection classified VAIJul 11, 201410 years or older, so it adds no points0
Inspection classified VAIJun 20, 201210 years or older, so it adds no points0
Inspection classified VAIJan 9, 200910 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
FUJIFILM Diosynth Biotechnologies UK Limited
Location
Billingham (GB)
Registration Expires
Dec 31, 2027
Operations
ANALYSIS; API MANUFACTURE
Source
decrs

Import refusals

FDA data resources

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