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
Madrid, Spain Not on file
SAN SEBASTIAN DE LOS REYES, 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

Questions about Farmasierra Manufacturing, S.L

Does Farmasierra Manufacturing, S.L hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Farmasierra Manufacturing, S.L. It does have 13 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Farmasierra Manufacturing, S.L FDA-registered?
One site operated by Farmasierra Manufacturing, 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 Farmasierra Manufacturing, S.L's last inspection go?
The most recent inspection on record closed on 18 January 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 2 inspections are on file.
Where does Farmasierra Manufacturing, S.L manufacture?
3 registered sites are on record, in Spain (Spain, Madrid and SAN Sebastian DE LOS Reyes). Every site is listed on this page with the register it came from.
Which regulators recognise Farmasierra Manufacturing, S.L's GMP?
Current GMP certificates are on record from ANVISA (Brazil), US FDA 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. 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.

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