Par Active Technologies Private Limited

FDA Regulatory Profile

Par Active Technologies Private Limited has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 4, 2025 · NAI

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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) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections6Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 4, 2025Alathur, IndiaDrugsNo Action Indicated (NAI)3003597293
Sep 27, 2019Alathur, IndiaDrugsNo Action Indicated (NAI)3003597293
Dec 1, 2017Alathur, IndiaDrugsVoluntary Action Indicated (VAI)3003597293
May 6, 2016Alathur, IndiaDrugsVoluntary Action Indicated (VAI)3003597293
May 21, 2012Alathur, IndiaDrugsVoluntary Action Indicated (VAI)3003597293
Jan 14, 2009Alathur, IndiaDrugsVoluntary Action Indicated (VAI)3003597293

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 3003597293Alathur, India6Jul 4, 2025

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