FDA Inspection 1148504 - Aesculap Inc - August 11, 2021

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Record Details

This FDA Inspection record concerns Aesculap Inc, with an inspection on August 11, 2021, issued by the Center for Devices and Radiological Health, covering devices.

Company: Aesculap Inc
Inspection Date: August 11, 2021
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1cada70d-7b1b-4a4c-ab7f-825bce159a0b

Violation Codes3

21 CFR 803.1721 CFR 803.50(a)(1)21 CFR 820.50(a)(1)

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