# FDA Inspection 1031064 - Medline Industries, Inc. - November 07, 2017

Source: https://www.keypedia.com/records/fda_inspections/medline-industries-inc/9d6a1d36-9d09-4e91-9bb6-3d06a5118f8d
Source feed: FDA_Inspections

> FDA Inspection 1031064 for Medline Industries, Inc. on November 07, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031064
- Company Name: Medline Industries, Inc.
- Inspection Date: 2017-11-07
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1031064 - 2017-11-07](https://www.keypedia.com/records/fda_inspections/medline-industries-inc/34530e8f-85d8-400e-a932-5e08e1c7f493)
- [FDA Inspection 721113 - 2011-04-29](https://www.keypedia.com/records/fda_inspections/medline-industries-inc/68798abf-6744-4b32-b268-0e674f57950f)
- [FDA Inspection 721113 - 2011-04-29](https://www.keypedia.com/records/fda_inspections/medline-industries-inc/b36ca861-76fc-4513-a275-4de03d3a1fc1)

Company: https://www.keypedia.com/companies/medline-industries-inc/77cbefc2-7e6d-465a-97a7-46c5ca1fc2c2

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