# FDA Inspection 1244696 - Pepin Manufacturing Inc - July 11, 2024

Source: https://www.keypedia.com/records/fda_inspections/pepin-manufacturing-inc/3c95acfa-ec8c-44c8-9d0f-af919cc151cc
Source feed: FDA_Inspections

> FDA Inspection 1244696 for Pepin Manufacturing Inc on July 11, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1244696
- Company Name: Pepin Manufacturing Inc
- Inspection Date: 2024-07-11
- 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 1244696 - 2024-07-11](https://www.keypedia.com/records/fda_inspections/pepin-manufacturing-inc/1e3cc397-cb92-4784-b4f8-51b7d1d23a48)
- [FDA Inspection 946537 - 2015-09-24](https://www.keypedia.com/records/fda_inspections/pepin-manufacturing-inc/897b59b9-4ca4-4ad7-9b1f-ce8486455d9a)
- [FDA Inspection 720391 - 2011-03-22](https://www.keypedia.com/records/fda_inspections/pepin-manufacturing-inc/50b58067-d633-40ef-b49e-e51a44c670ad)

Company: https://www.keypedia.com/companies/pepin-manufacturing-inc/d38b0d10-e76c-4f95-bd02-31cfaa715102

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