# FDA Inspection 753559 - Anchorplus - November 08, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/anchorplus/fda1885a-b392-4f7b-b164-0e4eed8d29f5/
Source feed: FDA_Inspections

> FDA Inspection 753559 for Anchorplus on November 08, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 753559
- Company Name: Anchorplus
- Inspection Date: 2011-11-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/anchorplus/abcb8a4c-0ea2-4959-aca1-1ebd433fd4da

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