Suppliers / Jurox Pty

Jurox Pty

Australia 57 employees Updated 9 July 2026

Jurox Pty is a finished-dose manufacturer based in Australia. It appears in 6 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with Health Canada and NPRA (MY). Its most recent recorded inspection, by US FDA, closed on 4 November 2011 as VAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
6
filings across 2 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

  • 4 November 2011 VAI US FDA

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

Registered plants

Site FDA FEI
Australia, Australia 3003483729

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 4 None
NPRA (MY) 2 None

Questions about Jurox Pty

Does Jurox Pty hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Jurox Pty. It does have 6 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Jurox Pty FDA-registered?
One site operated by Jurox Pty 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 Jurox Pty's last inspection go?
The most recent inspection on record closed on 4 November 2011 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does Jurox Pty manufacture?
1 registered site is on record, in Australia (Australia). Every site is listed on this page with the register it came from.
Where does Jurox Pty file?
Filings are on record with Health Canada and NPRA (MY), 6 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 4 November 2011.

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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