FDA Inspection 1278581 - Limerick Inc - August 15, 2025

FDA Inspection 1278581 for Limerick Inc on August 15, 2025. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1278581 for Limerick Inc on August 15, 2025. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.184

21 CFR 820.198(a)

21 CFR 820.90(a)

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Record Information

Company

Limerick Inc

Inspection Date

August 15, 2025

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa6304a8-9155-45d6-beb5-6aa3c781f9ca

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