# FDA Inspection 675392 - Therapak Corporation - June 29, 2010

Source: https://www.keypedia.com/records/fda_inspections/therapak-corporation/6acb5cf5-1c09-454c-86cf-717ce01ed423
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> FDA Inspection 675392 for Therapak Corporation on June 29, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 675392
- Company Name: Therapak Corporation
- Inspection Date: 2010-06-29
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/therapak-corporation/1a9ffab2-008a-4396-9e24-94bdc8fa916e

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