Steritech PTY. LTD.
FDA Regulatory Profile
Steritech PTY. LTD. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Jul 1, 2026 · VAI
Reviewing Steritech PTY. LTD. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Check this supplier
Or check Steritech PTY. LTD. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.
Get a free API key
Is this your company or a supplier you list? Link to this FDA record from your site with a free button.
Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 1 | Nov 11, 2026 | Newest record Nov 5, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Related names
| Name | Recalls | 510(k) | Inspections | Compliance | Most recent recall |
|---|
Steritech
Same company group | 0 | 0 | 6 | 0 | — |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|
| Jul 1, 2026 | Dandenong South, Australia | Devices | Voluntary Action Indicated (VAI) | 3002808271 |
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|
| FEI 3002808271 | Dandenong South, Australia | 1 | Jul 1, 2026 |