# The Procter & Gamble Manufacturing Company - Inspection Records

Source: https://www.globalkeysolutions.net/companies/the-procter-gamble-manufacturing-company/170695dc-3e07-442d-99c9-be48f302119f

> Inspection records and compliance data for The Procter & Gamble Manufacturing Company in West Branch, Iowa. Access full analysis and detailed observations.

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## Details

- Name: The Procter & Gamble Manufacturing Company
- FEI Number: 3004274728
- City: West Branch
- State: Iowa
- Country Name: United States
- Address Line 1: 160 Fawcett Dr
- Zip Code: 52358

## Related Documents

- [FDA Inspection 1146234 - The Procter & Gamble Manufacturing Company - 2021-07-12](https://www.globalkeysolutions.net/records/fda_inspections/the-procter-gamble-manufacturing-company/f81378b7-141e-41ff-a2f9-cb6e28206334) — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2021
- [FDA Inspection 1146234 - The Procter & Gamble Manufacturing Company - 2021-07-12](https://www.globalkeysolutions.net/records/fda_inspections/the-procter-gamble-manufacturing-company/f95e23ef-7fd0-40bb-9e1a-0f594e4613a4) — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2021
- [FDA Inspection 1146234 - The Procter & Gamble Manufacturing Company - 2021-07-12](https://www.globalkeysolutions.net/records/fda_inspections/the-procter-gamble-manufacturing-company/4d074b00-6dfe-48a4-a60a-c46f80aa9fdc) — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2021
- [FDA Inspection 1038651 - The Procter & Gamble Manufacturing Company - 2018-01-05](https://www.globalkeysolutions.net/records/fda_inspections/the-procter-gamble-manufacturing-company/19b410aa-36fd-4a31-9a88-87f211145e0f) — classification: No Action Indicated (NAI), source: FDA, date: January 5, 2018
- [FDA Inspection 845766 - The Procter & Gamble Manufacturing Company - 2013-07-30](https://www.globalkeysolutions.net/records/fda_inspections/the-procter-gamble-manufacturing-company/0ee47caf-88f4-49f3-8087-a68ccd7ce261) — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2013

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