Suppliers / Siegfried El Masnou

Siegfried El Masnou

Spain Updated 9 July 2026

The public registers hold a second record for Siegfried El Masnou. The fuller profile, with 94 active US DMFs and 40 valid CEPs, is at Siegfried. Figures on this page cover only this record.

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), EMA and AEMPS (ES). 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
EMA None 1
AEMPS (ES) None 1

Questions about Siegfried El Masnou

Does Siegfried El Masnou hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Siegfried El Masnou. It does have 4 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Siegfried El Masnou FDA-registered?
One site operated by Siegfried El Masnou carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Siegfried El Masnou's last inspection go?
The most recent inspection on record closed on 1 February 2023 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 5 inspections are on file.
Where does Siegfried El Masnou manufacture?
4 registered sites are on record, in United Arab Emirates and Spain (El Masnou (barcelona), Barcelona and El Masnou among others). Every site is listed on this page with the register it came from.
Which regulators recognise Siegfried El Masnou's GMP?
Current GMP certificates are on record from ANVISA (Brazil), EMA and AEMPS (ES). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

Comparing suppliers?

Choose your molecules and target markets. Siegfried El Masnou comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Open risk flags

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

Comparable suppliers

Alcaliber S A also in Spain Altan Pharmaceuticals also in Spain Berlimed also in Spain Casen Recordati, S.L also in Spain Cyndea Pharma, S.L also in Spain

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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