# FDA Inspection 1006768 - Patient Pocket LLC - February 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/patient-pocket-llc/98e490ea-4948-4e4a-a8b8-80adf207f7ff
Source feed: FDA_Inspections

> FDA Inspection 1006768 for Patient Pocket LLC on February 28, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1006768
- Company Name: Patient Pocket LLC
- Inspection Date: 2017-02-28
- 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 1119989 - 2020-01-27](https://www.keypedia.com/records/fda_inspections/patient-pocket-llc/4a1f222a-961f-47d9-b0d0-5958338b05dc)
- [FDA Inspection 1006768 - 2017-02-28](https://www.keypedia.com/records/fda_inspections/patient-pocket-llc/b553b97b-0f63-4282-a8fe-fe433f65ab1b)

Company: https://www.keypedia.com/companies/patient-pocket-llc/948a61b8-1387-4c81-af34-505803d6986c

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