# FDA Inspection 681275 - Longport, Inc - September 21, 2010

Source: https://www.keypedia.com/records/fda_inspections/longport-inc/b90a8c07-6283-4a5f-89eb-77fd594a00f9
Source feed: FDA_Inspections

> FDA Inspection 681275 for Longport, Inc on September 21, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 681275
- Company Name: Longport, Inc
- Inspection Date: 2010-09-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 681275 - 2010-09-21](https://www.keypedia.com/records/fda_inspections/longport-inc/ab5729fa-9d25-47ad-9bde-42e93aa93dcc)

Company: https://www.keypedia.com/companies/longport-inc/0ad50a42-ceea-421a-af68-140e6059d139

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