Suppliers / Maco Productions

Maco Productions

France Updated 9 July 2026

Maco Productions is a finished-dose manufacturer based in France. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file. Its most recent recorded inspection, by US FDA, closed on 12 September 2017 as VAI.

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

Inspection history

  • 12 September 2017 VAI US FDA

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

Registered plants

Site FDA FEI
France, France 3005138167

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 1 None

Questions about Maco Productions

Does Maco Productions hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Maco Productions. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Maco Productions FDA-registered?
One site operated by Maco Productions 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 Maco Productions's last inspection go?
The most recent inspection on record closed on 12 September 2017 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does Maco Productions manufacture?
1 registered site is on record, in France (France). Every site is listed on this page with the register it came from.
Where does Maco Productions file?
Filings are on record with US FDA, 1 in total.

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 12 September 2017.

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