Suppliers / Farmea

Farmea

France 90 employees Updated 9 July 2026

Farmea is a finished-dose manufacturer based in France. It appears in 6 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with NCELS (KZ), UZPHARM (UZ) and ARCSA (EC). Its GMP standing is certified by ANSM (FR), ANVISA (Brazil) and EAEU_EEC, among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 1 December 2022 as VAI.

0
active US DMFs
0
valid CEPs
2
registered plants 1 with an FDA FEI number
6
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
8 of 8 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 December 2022 VAI US FDA
  • 21 February 2019 VAI US FDA
  • 1 April 2016 VAI US FDA
  • 12 June 2015 VAI US FDA
  • 14 February 2014 VAI US FDA
  • 15 March 2013 VAI US FDA
  • 26 January 2012 NAI US FDA
  • 23 October 2008 NAI US FDA

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

Registered plants

Site FDA FEI
ANGERS, France Not on file
France, France 3003583056

Filings and GMP by regulator

Regulator Filings GMP certificates
NCELS (KZ) 3 None
UZPHARM (UZ) 2 None
ARCSA (EC) 1 None
ANSM (FR) None 9
ANVISA (Brazil) None 2
EAEU_EEC None 1
EMA None 1

Scale

Year Revenue Exports Destinations
2024 $81.5M Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

Questions about Farmea

Does Farmea hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Farmea. It does have 6 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Farmea FDA-registered?
One site operated by Farmea 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 Farmea's last inspection go?
The most recent inspection on record closed on 1 December 2022 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 8 inspections are on file.
Where does Farmea manufacture?
2 registered sites are on record, in France (Angers and France). Every site is listed on this page with the register it came from.
Which regulators recognise Farmea's GMP?
Current GMP certificates are on record from ANSM (FR), ANVISA (Brazil), EEC (Eurasian Economic Union) and EMA. 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 1 December 2022.

Comparable suppliers

AdhexPharma also in France Advanced Accelerator Applications also in France Aspen Notre Dame De Bondeville also in France Astrazeneca Dunkerque Production also in France Astrea Fontaine also in France

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
Company filings
Revenue as reported