# FDA Inspection 1112351 - Keystone Manufacturing LLC. - December 11, 2019

Source: https://www.keypedia.com/records/fda_inspections/keystone-manufacturing-llc/1bf0ccde-11e9-4e50-b5f1-687cac77e59b
Source feed: FDA_Inspections

> FDA Inspection 1112351 for Keystone Manufacturing LLC. on December 11, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1112351
- Company Name: Keystone Manufacturing LLC.
- Inspection Date: 2019-12-11
- 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 1112351 - 2019-12-11](https://www.keypedia.com/records/fda_inspections/keystone-manufacturing-llc/727b4f44-0b44-4fb7-9ac7-089b035dd8b9)
- [FDA Inspection 765632 - 2012-01-24](https://www.keypedia.com/records/fda_inspections/keystone-manufacturing-llc/aa0ee3a6-fcc8-465b-a4d0-9fc25c441f6c)

Company: https://www.keypedia.com/companies/keystone-manufacturing-llc/7ea1e876-c62d-4547-a081-97d9ec12d7ba

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