# FDA Inspection 1066964 - LILMO Ltd. - September 12, 2018

Source: https://www.keypedia.com/records/fda_inspections/lilmo-ltd/03540657-e53d-40f8-84f8-e0dca6cfa069
Source feed: FDA_Inspections

> FDA Inspection 1066964 for LILMO Ltd. on September 12, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066964
- Company Name: LILMO Ltd.
- Inspection Date: 2018-09-12
- 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 1066964 - 2018-09-12](https://www.keypedia.com/records/fda_inspections/lilmo-ltd/d87532e6-0724-4959-9c81-f7c8c3308464)

Company: https://www.keypedia.com/companies/lilmo-ltd/ac081dd3-e5ab-4786-9957-97f077265385

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