# FDA Inspection 1057152 - Primrose Medical Inc. - June 06, 2018

Source: https://www.keypedia.com/records/fda_inspections/primrose-medical-inc/29840be9-d602-45d7-a207-ab77692b1bea
Source feed: FDA_Inspections

> FDA Inspection 1057152 for Primrose Medical Inc. on June 06, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1057152
- Company Name: Primrose Medical Inc.
- Inspection Date: 2018-06-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1057152 - 2018-06-06](https://www.keypedia.com/records/fda_inspections/primrose-medical-inc/4f0d1d2b-a38f-450c-9122-84a438eae5ea)

Company: https://www.keypedia.com/companies/primrose-medical-inc/183a9d6e-b369-4fad-9cf6-a3f528b076a3

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