Suppliers / Deretil

Deretil

Spain Updated 9 July 2026

Deretil is an API manufacturer based in Spain. Its most recent recorded inspection, by US FDA, closed on 24 March 2023 as VAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
5 of 5 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 24 March 2023 VAI US FDA
  • 13 March 2019 VAI US FDA
  • 8 January 2016 NAI US FDA
  • 26 September 2013 VAI US FDA
  • 1 July 2010 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Spain, Spain 3003747614

What they file, and where

Molecule Regulators Docs
Amoxicillin SFDA (Saudi Arabia) 2

Also appears on these molecule pages

Amoxicillin API

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Open risk flags

  • The most recent inspection outcome was VAI, on 24 March 2023.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability