# FDA Inspection 1224005 - Micropen Technologies - November 14, 2023

Source: https://www.keypedia.com/records/fda_inspections/micropen-technologies/44f3647b-a54d-419a-82ce-bb93eb9db945
Source feed: FDA_Inspections

> FDA Inspection 1224005 for Micropen Technologies on November 14, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1224005
- Company Name: Micropen Technologies
- Inspection Date: 2023-11-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1224005 - 2023-11-14](https://www.keypedia.com/records/fda_inspections/micropen-technologies/53969357-1585-4730-90da-091b0a42ab6c)
- [FDA Inspection 1153364 - 2021-09-24](https://www.keypedia.com/records/fda_inspections/micropen-technologies/16ab8d6f-8d9c-4930-920d-bff6b01d6c51)
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- [FDA Inspection 1071858 - 2018-11-14](https://www.keypedia.com/records/fda_inspections/micropen-technologies/70a0c1b9-e42d-4ac9-8693-3f3586a6ecb9)

Company: https://www.keypedia.com/companies/micropen-technologies/c94ac8d5-1102-4376-b814-e8949bcd4040

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