# FDA Inspection 625087 - Atlantic Ultraviolet - November 02, 2009

Source: https://www.keypedia.com/records/fda_inspections/atlantic-ultraviolet/8db76f76-2117-4dcc-97d4-57d7ba8424ec
Source feed: FDA_Inspections

> FDA Inspection 625087 for Atlantic Ultraviolet on November 02, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 625087
- Company Name: Atlantic Ultraviolet
- Inspection Date: 2009-11-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/atlantic-ultraviolet/449ac45b-2996-485d-aab9-d85df676b997

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