# FDA Inspection 840750 - Lake City Products - July 17, 2013

Source: https://www.keypedia.com/records/fda_inspections/lake-city-products/0201395b-46dc-46d5-addc-c623d8f5aa91
Source feed: FDA_Inspections

> FDA Inspection 840750 for Lake City Products on July 17, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 840750
- Company Name: Lake City Products
- Inspection Date: 2013-07-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 840750 - 2013-07-17](https://www.keypedia.com/records/fda_inspections/lake-city-products/6b28824c-5a3b-47ac-89a4-167d602f6c77)

Company: https://www.keypedia.com/companies/lake-city-products/b1e315fd-a531-4c3c-97d5-4c2e21a18e97

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