Suppliers / Farmasierra Manufacturing, S.L

Farmasierra Manufacturing, S.L

Spain Updated 9 July 2026

Farmasierra Manufacturing, S.L is a finished-dose manufacturer based in Spain. It appears in 13 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with EEC_EAEU, DIGEMAPS (DO) and MINSA (CR). Its GMP standing is certified by ANVISA (Brazil), US FDA and AEMPS (ES). Its most recent recorded inspection, by US FDA, closed on 18 January 2024 as VAI.

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
13
filings across 5 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
2 of 2 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 18 January 2024 VAI US FDA
  • 30 January 2020 NAI 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 3007898507
SAN SEBASTIAN DE LOS REYES, Spain Not on file
Madrid, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EEC_EAEU 5 None
DIGEMAPS (DO) 3 None
MINSA (CR) 3 None
JFDA (JO) 1 None
ARCSA (EC) 1 None
ANVISA (Brazil) None 2
US FDA None 1
AEMPS (ES) None 1

Comparing suppliers?

Choose your molecules and target markets. Farmasierra Manufacturing, S.L 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 18 January 2024.

Sources on this page

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