# FDA Inspection 1205347 - Interscope, Inc. - May 05, 2023

Source: https://www.keypedia.com/records/fda_inspections/interscope-inc/b880ee18-8e6f-4718-8420-3ddfcd36bd63
Source feed: FDA_Inspections

> FDA Inspection 1205347 for Interscope, Inc. on May 05, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1205347
- Company Name: Interscope, Inc.
- Inspection Date: 2023-05-05
- 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 1205347 - 2023-05-05](https://www.keypedia.com/records/fda_inspections/interscope-inc/760b291c-b9e3-4530-947f-f4135b1464ae)
- [FDA Inspection 1087178 - 2019-04-22](https://www.keypedia.com/records/fda_inspections/interscope-inc/089525ff-528f-4628-9321-e13e023fd257)
- [FDA Inspection 1087178 - 2019-04-22](https://www.keypedia.com/records/fda_inspections/interscope-inc/c1cd2b94-2757-41b4-9043-0ceb66713c28)

Company: https://www.keypedia.com/companies/interscope-inc/bd9438fe-6dcd-4df7-ae00-4418482fc4c1

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