# FDA Inspection 1062209 - Anutra Medical Inc - August 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/anutra-medical-inc/21ff6941-d2dc-4229-81d6-1d1a789e9908
Source feed: FDA_Inspections

> FDA Inspection 1062209 for Anutra Medical Inc on August 15, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1062209
- Company Name: Anutra Medical Inc
- Inspection Date: 2018-08-15
- 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 1062209 - 2018-08-15](https://www.keypedia.com/records/fda_inspections/anutra-medical-inc/8aa91f6c-f9c5-45af-9650-c2e7174e376d)

Company: https://www.keypedia.com/companies/anutra-medical-inc/d34eab84-8047-40b5-bf42-f7d96c6681c2

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