Martin Pleasance Manufacturing Pty Ltd
FDA import alert and refusal historyLoganholme, AustraliaFEI 3031922136
Recorded by FDA as MARTIN PLEASANCE MANUFACTURING PTY LTD
As of October 26, 2026, Martin Pleasance Manufacturing Pty Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 14, 2025, most often for insanitary conditions, may be injurious (MFR INJ).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Herbals & botanicals (not teas), n.e.c. · MFR INJ
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Martin Pleasance Manufacturing Pty Ltd
1 record, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- MFR INJ1 refused line
Insanitary conditions, may be injurious
The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.
Questions about Martin Pleasance Manufacturing Pty Ltd
- Is Martin Pleasance Manufacturing Pty Ltd on an FDA import alert?
- No listing for Martin Pleasance Manufacturing Pty Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Australia page.
- Has FDA refused shipments from Martin Pleasance Manufacturing Pty Ltd?
- Yes. FDA refused 1 shipment line from Martin Pleasance Manufacturing Pty Ltd on May 14, 2025. The most recent, on May 14, 2025, was herbals & botanicals (not teas), n.e.c., charged as MFR INJ (insanitary conditions, may be injurious).
- Why did FDA refuse Martin Pleasance Manufacturing Pty Ltd's shipments?
- The most frequent charge is MFR INJ (insanitary conditions, may be injurious, 1 line).
- What is Martin Pleasance Manufacturing Pty Ltd's FEI number?
- Martin Pleasance Manufacturing Pty Ltd's FDA Establishment Identifier (FEI) is 3031922136.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.