# FDA Inspection 1008076 - Sanford L.P. - March 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/sanford-lp/a9de6c74-650e-4f57-8ff7-31f198606ae6
Source feed: FDA_Inspections

> FDA Inspection 1008076 for Sanford L.P. on March 24, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008076
- Company Name: Sanford L.P.
- Inspection Date: 2017-03-24
- 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/sanford-lp/feead519-d7ae-4818-9bd7-7f7b1b9a1bd5

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