# FDA Inspection 803237 - Mobisante, Inc - October 16, 2012

Source: https://www.keypedia.com/records/fda_inspections/mobisante-inc/a5cedb7c-e641-481e-a39f-b0330e94c4a4
Source feed: FDA_Inspections

> FDA Inspection 803237 for Mobisante, Inc on October 16, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803237
- Company Name: Mobisante, Inc
- Inspection Date: 2012-10-16
- 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 803237 - 2012-10-16](https://www.keypedia.com/records/fda_inspections/mobisante-inc/64b8b3ee-31b7-419a-b97e-0fb5ac4524ff)

Company: https://www.keypedia.com/companies/mobisante-inc/46230b47-9ba1-40a6-8318-db1d47d2ce4c

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