Suppliers / Siegfried El Masnou

Siegfried El Masnou

Spain Updated 9 July 2026

Siegfried El Masnou is a finished-dose manufacturer based in Spain. It appears in 4 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDE (AE), NCELS (KZ) and NPRA (MY). Its GMP standing is certified by ANVISA (Brazil), AEMPS (ES) and EMA. Its most recent recorded inspection, by US FDA, closed on 1 February 2023 as VAI.

0
active US DMFs
0
valid CEPs
4
registered plants 1 with an FDA FEI number
4
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
5 of 5 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 1 February 2023 VAI US FDA
  • 31 January 2019 VAI US FDA
  • 3 July 2015 NAI US FDA
  • 5 July 2013 NAI US FDA
  • 9 September 2011 VAI US FDA

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

Registered plants

Site FDA FEI
El Masnou (Barcelona), United Arab Emirates Not on file
BARCELONA, Spain Not on file
El Masnou, Spain Not on file
Spain, Spain 3002894596

Filings and GMP by regulator

Regulator Filings GMP certificates
EDE (AE) 2 None
NCELS (KZ) 1 None
NPRA (MY) 1 None
ANVISA (Brazil) None 1
AEMPS (ES) None 1
EMA None 1

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Open risk flags

  • The most recent inspection outcome was VAI, on 1 February 2023.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates