Wardray Premise, Ltd.

FDA Regulatory Profile

Wardray Premise, Ltd. has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Jan 9, 2025 · OAI
Latest 510(k)
Dec 21, 2012

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances1Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 9, 2025Brighouse, United KingdomDevicesOfficial Action Indicated (OAI)3009530228
Oct 13, 2017Sutton, United KingdomDevicesVoluntary Action Indicated (VAI)3007912863

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

FacilityLocationInspectionsLatest
FEI 3009530228Brighouse, United Kingdom1Jan 9, 2025
FEI 3007912863Sutton, United Kingdom1Oct 13, 2017

Recent 510(k) Clearances

K-NumberDeviceDate
K120391MR4500 WHEELCHAIRDec 21, 2012

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.