FUJIFILM Diosynth Biotechnologies UK Ltd

FDA inspection history in Billingham, United Kingdom, 2023

1
Form 483

Every document, by year

  • Form 483

2023: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2023One Form 483, at Billingham, United Kingdom.

Cited most

Across all FUJIFILM Diosynth Biotechnologies UK observations on file

The complete FUJIFILM Diosynth Biotechnologies UK file.

All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.

$99

The documents one by one, while the file is prepared

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Sites

Documents

1 on file, newest first
DateDocumentPrice
2023-03-17483 Form 483$99

Investigators on these documents

Libia M. Lugo (1)

FEI number 3007182567 · most recent document Mar 17, 2023

About FUJIFILM Diosynth Biotechnologies UK Ltd

How many FDA Form 483s has FUJIFILM Diosynth Biotechnologies UK Ltd received?

FDA Intel has 1 Form 483 on file for FUJIFILM Diosynth Biotechnologies UK Ltd; the most recent is dated Mar 17, 2023.

When was FUJIFILM Diosynth Biotechnologies UK Ltd last inspected by FDA?

The most recent FDA inspection document on file for FUJIFILM Diosynth Biotechnologies UK Ltd is a Form 483 dated Mar 17, 2023, for the site in Billingham, United Kingdom.

What did FDA cite at FUJIFILM Diosynth Biotechnologies UK Ltd?

The regulations cited most in the observations on file for FUJIFILM Diosynth Biotechnologies UK Ltd are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.113 (Control of microbiological contamination), 1 time.