# FDA Inspection 978322 - Therapak LLC - June 30, 2016

Source: https://www.keypedia.com/records/fda_inspections/therapak-llc/07495a1a-8c94-4199-b06f-378a914325e8
Source feed: FDA_Inspections

> FDA Inspection 978322 for Therapak LLC on June 30, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 978322
- Company Name: Therapak LLC
- Inspection Date: 2016-06-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/therapak-llc/be30daab-38da-49aa-a000-9ad1b641738e

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