# FDA Inspection 582163 - The Procter & Gamble Co. - April 24, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/the-procter-gamble-co/30bbb46d-9cb6-4c06-a095-7d105c3ce176
Source feed: FDA_Inspections

> FDA Inspection 582163 for The Procter & Gamble Co. on April 24, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 582163
- Company Name: The Procter & Gamble Co.
- Inspection Date: 2009-04-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1020805 - 2017-06-22](https://www.globalkeysolutions.net/records/fda_inspections/the-procter-gamble-co/dc01d497-3ed3-4399-bef2-3a4cfd0b648c)
- [FDA Inspection 1020805 - 2017-06-22](https://www.globalkeysolutions.net/records/fda_inspections/the-procter-gamble-co/028f795c-56b2-4186-b7bc-76f630dc823d)
- [FDA Inspection 880491 - 2014-06-02](https://www.globalkeysolutions.net/records/fda_inspections/the-procter-gamble-co/6f608e63-8c36-42e0-a499-f7bb6063ab61)
- [FDA Inspection 814797 - 2012-11-26](https://www.globalkeysolutions.net/records/fda_inspections/the-procter-gamble-co/cd00e37e-5f3b-45f8-b97b-9465f9c15b01)

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