# FDA Inspection 1201082 - Daily Medical Products, Inc. - March 21, 2023

Source: https://www.keypedia.com/records/fda_inspections/daily-medical-products-inc/4bd4da5b-341a-4890-add5-8d8184d65d92
Source feed: FDA_Inspections

> FDA Inspection 1201082 for Daily Medical Products, Inc. on March 21, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1201082
- Company Name: Daily Medical Products, Inc.
- Inspection Date: 2023-03-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1201082 - 2023-03-21](https://www.keypedia.com/records/fda_inspections/daily-medical-products-inc/b195cf24-e9c7-473c-a9a3-bcfb278c14d3)
- [FDA Inspection 1016104 - 2017-04-06](https://www.keypedia.com/records/fda_inspections/daily-medical-products-inc/cac0aa73-50ed-4560-a3fc-2617501a255a)
- [FDA Inspection 853083 - 2013-10-29](https://www.keypedia.com/records/fda_inspections/daily-medical-products-inc/841b773f-60dc-462f-be26-6e912da8ab26)
- [FDA Inspection 724943 - 2011-05-05](https://www.keypedia.com/records/fda_inspections/daily-medical-products-inc/cfa2a5a7-3871-4429-adf8-8edf05b5da90)

Company: https://www.keypedia.com/companies/daily-medical-products-inc/7ac88fcf-46ca-493f-b8d9-92cf54b7b4bd

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