CCRM Seattle LLC

FDA Regulatory Profile

CCRM Seattle LLC has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 13, 2026 · 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
Inspections7Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 13, 2026Bellevue, WABiologicsVoluntary Action Indicated (VAI)3004174071
Mar 23, 2023Bellevue, WABiologicsNo Action Indicated (NAI)3004174071
Sep 27, 2017Bellevue, WABiologicsNo Action Indicated (NAI)3004174071
Apr 19, 2016Bellevue, WABiologicsVoluntary Action Indicated (VAI)3004174071
Dec 9, 2014Bellevue, WABiologicsVoluntary Action Indicated (VAI)3004174071
Jan 17, 2014Bellevue, WABiologicsVoluntary Action Indicated (VAI)3004174071
Jan 5, 2011Bellevue, WABiologicsNo Action Indicated (NAI)3004174071

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 3004174071Bellevue, WA7Aug 13, 2026

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