Suppliers / Siegfried Barbera S.L

Siegfried Barbera S.L

Spain 2 duplicate records merged Updated 9 July 2026

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

Siegfried Barbera S.L is a finished-dose manufacturer based in Spain. It appears in 31 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with MINSA (CR), ARCSA (EC) and UZPHARM (UZ). Its GMP standing is certified by ANVISA (Brazil), MFDS (Korea) and EMA, among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 30 March 2023 as VAI.

0
active US DMFs
0
valid CEPs
5
registered plants 1 with an FDA FEI number
31
filings across 5 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
3 of 3 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

  • 30 March 2023 VAI US FDA
  • 11 October 2018 VAI US FDA
  • 18 July 2014 NAI US FDA

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

Registered plants

Site FDA FEI
Barbera del Valles (Barcelona), United Arab Emirates Not on file
BARCELONA, Spain Not on file
Barcelona, Spain Not on file
Barbera Del Valles, Spain Not on file
Spain, Spain 3002910506

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 13 None
ARCSA (EC) 7 None
UZPHARM (UZ) 5 None
NCELS (KZ) 4 None
DIGEMAPS (DO) 2 None
ANVISA (Brazil) None 3
MFDS (Korea) None 2
EMA None 2
AEMPS (ES) None 1

Questions about Siegfried Barbera S.L

Does Siegfried Barbera S.L hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Siegfried Barbera S.L. It does have 31 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Siegfried Barbera S.L FDA-registered?
One site operated by Siegfried Barbera S.L 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 Barbera S.L's last inspection go?
The most recent inspection on record closed on 30 March 2023 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 3 inspections are on file.
Where does Siegfried Barbera S.L manufacture?
5 registered sites are on record, in United Arab Emirates and Spain (Barbera Del Valles (barcelona), Barcelona and Barcelona among others). Every site is listed on this page with the register it came from.
Which regulators recognise Siegfried Barbera S.L's GMP?
Current GMP certificates are on record from ANVISA (Brazil), MFDS (Korea), 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.

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Open risk flags

  • The most recent inspection outcome was VAI, on 30 March 2023.

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Sources on this page

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