# FDA Inspection 592207 - Lofton Label, Inc. - June 18, 2009

Source: https://www.keypedia.com/records/fda_inspections/lofton-label-inc/6b23481b-da55-4ccb-b0eb-3b7a8d6a5c2a
Source feed: FDA_Inspections

> FDA Inspection 592207 for Lofton Label, Inc. on June 18, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 592207
- Company Name: Lofton Label, Inc.
- Inspection Date: 2009-06-18
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/lofton-label-inc/4beb7bc1-b81c-4e06-aef4-582494b5a598

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