Vilvet Pharmaceuticals Inc.

FDA Regulatory Profile

Vilvet Pharmaceuticals Inc. has 2 FDA recalls, 1 inspection, 0 510(k) clearances and 1 compliance action on record.

Latest recall
D-1487-2020 · Class II · Jul 24, 2020
Latest inspection
Jun 27, 2018 · OAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls2Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
D-1487-2020Class IIVILAMIT MB (118 mg methenamine, 36 mg phenyl salicylate, 40.8 mg sodium phosphate monobasic, 10.0 mg…Jul 24, 2020
D-1488-2020Class IIVILEVEV MB Urinary Antispetic (81.0 mg methenamine, 40.8 mg sodium phosphate monobasic and 10.8 mg…Jul 24, 2020

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 27, 2018Chester Springs, PADrugsOfficial Action Indicated (OAI)3013511339

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 3013511339Chester Springs, PA1Jun 27, 2018

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