Suppliers / Grimann, S.A. de C.V

Grimann, S.A. de C.V

Mexico Updated 9 July 2026

Grimann, S.A. de C.V is a finished-dose manufacturer based in Mexico. It appears in 25 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with MINSA (CR), DIGEMAPS (DO) and ARCSA (EC). Its GMP standing is certified by COFEPRIS (MX) and INVIMA (CO). Customs aggregates show $195K of exports covering 1 molecule to 1 destination in 2023.

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

Registered plants

Site FDA FEI
Lerma Estado De Mexico, Colombia Not on file
Lerma, Mexico Not on file
Mexico, Mexico 3006076347

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 11 None
DIGEMAPS (DO) 8 None
ARCSA (EC) 4 None
COFEPRIS (MX) 2 4
INVIMA (CO) None 1

Scale

Year Revenue Exports Destinations
2023 Not reported $195K 1
2022 Not reported $864K 1

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Grimann, S.A. de C.V

Does Grimann, S.A. de C.V hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Grimann, S.A. de C.V. It does have 25 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Grimann, S.A. de C.V FDA-registered?
One site operated by Grimann, S.A. de C.V 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.
Where does Grimann, S.A. de C.V manufacture?
3 registered sites are on record, in Colombia and Mexico (Lerma Estado De Mexico, Lerma and Mexico). Every site is listed on this page with the register it came from.
Which regulators recognise Grimann, S.A. de C.V's GMP?
Current GMP certificates are on record from COFEPRIS (MX) and INVIMA (CO). 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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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
Customs aggregates
Export values, molecule and destination counts