FDA Inspection 848920 - Moog Costa Rica, SRL - September 19, 2013

FDA Inspection 848920 for Moog Costa Rica, SRL on September 19, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 848920 for Moog Costa Rica, SRL on September 19, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.40

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Record Information

Company

Moog Costa Rica, SRL

Inspection Date

September 19, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fca86433-63ea-41a1-a6f4-8e8a86a9ea63

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