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

Source: https://www.globalkeysolutions.net/records/fda_inspections/the-procter-gamble-co/dc01d497-3ed3-4399-bef2-3a4cfd0b648c
Source feed: FDA_Inspections

> FDA Inspection 1020805 for The Procter & Gamble Co. on June 22, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020805
- Company Name: The Procter & Gamble Co.
- Inspection Date: 2017-06-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/the-procter-gamble-co/206fbe2e-4b0a-4555-b701-c4b88baddbdb

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7