# FDA Inspection 1123140 - Therapak LLC - March 02, 2020

Source: https://www.keypedia.com/records/fda_inspections/therapak-llc/4764fec7-c989-43ef-ae36-552c38c1afcb
Source feed: FDA_Inspections

> FDA Inspection 1123140 for Therapak LLC on March 02, 2020. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1123140
- Company Name: Therapak LLC
- Inspection Date: 2020-03-02
- 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 1123140 - 2020-03-02](https://www.keypedia.com/records/fda_inspections/therapak-llc/d0159c8b-c2c4-4140-bc4b-4eb1ad773e3a)
- [FDA Inspection 978322 - 2016-06-30](https://www.keypedia.com/records/fda_inspections/therapak-llc/07495a1a-8c94-4199-b06f-378a914325e8)

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