# Longport, Inc – FDA Inspection, Sep 21, 2010

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

> FDA inspection 681275 of Longport, Inc, September 21, 2010. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

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