Candler Hospital Inc

FDA Regulatory Profile

Candler Hospital Inc has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 30, 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
Inspections7Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 30, 2025Savannah, GABiologicsNo Action Indicated (NAI)1073866
Apr 19, 2023Savannah, GABiologicsNo Action Indicated (NAI)1073866
Feb 8, 2018Savannah, GABiologicsNo Action Indicated (NAI)1073866
Aug 12, 2016Savannah, GABiologicsNo Action Indicated (NAI)1073866
Feb 20, 2014Savannah, GABiologicsNo Action Indicated (NAI)1073866
May 25, 2012Savannah, GABiologicsNo Action Indicated (NAI)1073866
Nov 3, 2010Savannah, GABiologicsNo Action Indicated (NAI)1073866

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 1073866Savannah, GA7Jul 30, 2025

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