# FDA Inspection 833822 - Litecure LLC - May 23, 2013

Source: https://www.keypedia.com/records/fda_inspections/litecure-llc/c97b65d5-a9c3-4934-8c30-e45eed0ce246
Source feed: FDA_Inspections

> FDA Inspection 833822 for Litecure LLC on May 23, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 833822
- Company Name: Litecure LLC
- Inspection Date: 2013-05-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 833822 - 2013-05-23](https://www.keypedia.com/records/fda_inspections/litecure-llc/2aa82eab-f7fd-41c8-b413-42931b8a753c)
- [FDA Inspection 833822 - 2013-05-23](https://www.keypedia.com/records/fda_inspections/litecure-llc/a5c7146c-d9dc-4be0-b66e-7b592a8b99cc)

Company: https://www.keypedia.com/companies/litecure-llc/dbb98b56-6ea6-46ba-8651-9e266cb11708

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