# FDA Inspection 608187 - Clearwater Products, LLC - August 25, 2009

Source: https://www.keypedia.com/records/fda_inspections/clearwater-products-llc/d8defb68-a897-4a98-aa1d-9579bf1ca2a9
Source feed: FDA_Inspections

> FDA Inspection 608187 for Clearwater Products, LLC on August 25, 2009. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 608187
- Company Name: Clearwater Products, LLC
- Inspection Date: 2009-08-25
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 697635 - 2010-11-15](https://www.keypedia.com/records/fda_inspections/clearwater-products-llc/401b1743-553e-4986-837f-3e891a739f6d)
- [FDA Inspection 697635 - 2010-11-15](https://www.keypedia.com/records/fda_inspections/clearwater-products-llc/a5972551-949c-47bb-9f8f-53db7834de97)
- [FDA Inspection 608187 - 2009-08-25](https://www.keypedia.com/records/fda_inspections/clearwater-products-llc/a2fb5eee-af70-43cd-b478-c976c2078e6d)

Company: https://www.keypedia.com/companies/clearwater-products-llc/e93679b5-9d67-4660-a050-f7c80029e716

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