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Pacific BioLabs, Inc.

FDA Regulatory Profile

Pacific BioLabs, Inc. has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 18, 2025 · VAI

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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
Inspections9Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 18, 2025Hercules, CADrugsVoluntary Action Indicated (VAI)2914117
Jun 1, 2023Hercules, CADrugsVoluntary Action Indicated (VAI)2914117
Mar 19, 2018Hercules, CADrugsVoluntary Action Indicated (VAI)2914117
Oct 30, 2013Hercules, CADrugsVoluntary Action Indicated (VAI)2914117
Oct 19, 2010Hercules, CADrugsNo Action Indicated (NAI)2914117
May 24, 2010Hercules, CADrugsNo Action Indicated (NAI)2914117
Sep 18, 2009Hercules, CADrugsNo Action Indicated (NAI)2914117
Sep 9, 2009Hercules, CADrugsNo Action Indicated (NAI)2914117
Jun 4, 2009Hercules, CADrugsNo Action Indicated (NAI)2914117

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 2914117Hercules, CA9Jul 18, 2025

FDA data resources

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