Suppliers / Sourcetech Quimica Ltda

Sourcetech Quimica Ltda

Brazil Updated 9 July 2026

Sourcetech Quimica Ltda is an API manufacturer based in Brazil. It holds one active US drug master file and 2 valid CEPs. Its most recent recorded inspection, by US FDA, closed on 3 June 2022 as VAI.

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

Inspection history

  • 3 June 2022 VAI US FDA
  • 11 March 2016 VAI US FDA
  • 30 November 2012 VAI US FDA

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

Registered plants

Site FDA FEI
Pindamonhangaba, Brazil Not on file
Brazil, Brazil 1000571090

What they file, and where

Molecule Regulators Docs
Pilocarpine EDQM, US FDA 3

Questions about Sourcetech Quimica Ltda

Does Sourcetech Quimica Ltda hold a US DMF or a CEP?
Sourcetech Quimica Ltda holds 1 active US drug master file and 2 valid CEPs. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is Sourcetech Quimica Ltda FDA-registered?
One site operated by Sourcetech Quimica Ltda 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 Sourcetech Quimica Ltda's last inspection go?
The most recent inspection on record closed on 3 June 2022 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 3 inspections are on file.
Where does Sourcetech Quimica Ltda manufacture?
2 registered sites are on record, in Brazil (Pindamonhangaba and Brazil). Every site is listed on this page with the register it came from.
What does Sourcetech Quimica Ltda make?
1 molecule is on record against Sourcetech Quimica Ltda, including Pilocarpine. Each links through to that molecule's full manufacturer list.

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 3 June 2022.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability