# FDA Inspection 830604 - Lazarus Effect Inc - May 06, 2013

Source: https://www.keypedia.com/records/fda_inspections/lazarus-effect-inc/eb05a7c7-e0bd-4a12-b2b9-add89e8690fb
Source feed: FDA_Inspections

> FDA Inspection 830604 for Lazarus Effect Inc on May 06, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 830604
- Company Name: Lazarus Effect Inc
- Inspection Date: 2013-05-06
- 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 830604 - 2013-05-06](https://www.keypedia.com/records/fda_inspections/lazarus-effect-inc/978684f7-35be-4a53-96c2-8567af0ac52b)

Company: https://www.keypedia.com/companies/lazarus-effect-inc/fd07f923-89a7-4e98-8e34-a9f038a33c9d

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