Bahadir USA Corp.

FDA Regulatory Profile

Bahadir USA Corp. appears in FDA public data with 0 recalls, 4 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent FDA inspection ended on Jul 17, 2023 (No Action Indicated (NAI)). Its most recent 510(k) clearance was granted on Mar 22, 2024.

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Summary

Total Recalls
0
510(k) Clearances
4
Inspections
3
Compliance Actions
0

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 17, 2023Carneys Point, NJDevicesNo Action Indicated (NAI)3005741909
Sep 21, 2016Carneys Point, NJDevicesNo Action Indicated (NAI)3005741909
Oct 28, 2013Carneys Point, NJDevicesNo Action Indicated (NAI)3005741909

FDA Data Dashboard classifications: NAI (no action indicated), VAI (voluntary action indicated), OAI (official action indicated).

Recent 510(k) Clearances

K-NumberDeviceDate
K233578BAHADIR STERILIZATION CONTAINERSMar 22, 2024
K131407BAHADIR STERILIZATION TRAYSAug 12, 2014
K112090BAHADIR STERILIZATION TRAYSJun 7, 2012
K102146BAHADIR STERILIZATION TRAYSNov 18, 2010