FDA Inspection 1020805 - The Procter & Gamble Co. - June 22, 2017

Record Details

This FDA Inspection record concerns The Procter & Gamble Co., with an inspection on June 22, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: The Procter & Gamble Co.
Inspection Date: June 22, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · dc01d497-3ed3-4399-bef2-3a4cfd0b648c