# FDA Inspection 610768 - SwimEx, Incorporated - September 09, 2009

Source: https://www.keypedia.com/records/fda_inspections/swimex-incorporated/0e57726e-2b78-4f33-8b74-f05efff962fb
Source feed: FDA_Inspections

> FDA Inspection 610768 for SwimEx, Incorporated on September 09, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 610768
- Company Name: SwimEx, Incorporated
- Inspection Date: 2009-09-09
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 810908 - 2012-11-21](https://www.keypedia.com/records/fda_inspections/swimex-incorporated/189693e4-4284-41db-ad4c-3601c4dba990)
- [FDA Inspection 610768 - 2009-09-09](https://www.keypedia.com/records/fda_inspections/swimex-incorporated/bcdd76aa-06b1-44b4-8fc8-3eda7af93c06)

Company: https://www.keypedia.com/companies/swimex-incorporated/472c14b0-6dff-42e9-843a-01b55ee08cd7

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