# FDA Inspection 1028322 - Ameda, Inc. - September 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/ameda-inc/62ee4e2a-7921-42c0-b841-c8b1617d1643
Source feed: FDA_Inspections

> FDA Inspection 1028322 for Ameda, Inc. on September 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028322
- Company Name: Ameda, Inc.
- Inspection Date: 2017-09-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1028322 - 2017-09-21](https://www.keypedia.com/records/fda_inspections/ameda-inc/31aaa760-a676-4d1d-a693-6a5b556d483c)

Company: https://www.keypedia.com/companies/ameda-inc/b513c2fe-0a9a-4361-a7a1-1646084be158

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