# FDA Inspection 1205472 - Geneoscopy, Inc. - May 17, 2023

Source: https://www.keypedia.com/records/fda_inspections/geneoscopy-inc/a416b54d-d22f-4a2b-8b64-85d4419b7431
Source feed: FDA_Inspections

> FDA Inspection 1205472 for Geneoscopy, Inc. on May 17, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1205472
- Company Name: Geneoscopy, Inc.
- Inspection Date: 2023-05-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/geneoscopy-inc/b70bf3df-90bb-48eb-8f65-c2cb50441be4

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