# FDA Inspection 1060039 - Forge Medical Inc. - July 18, 2018

Source: https://www.keypedia.com/records/fda_inspections/forge-medical-inc/b2070cfc-7a2d-4f81-be41-a5dd68fb18df
Source feed: FDA_Inspections

> FDA Inspection 1060039 for Forge Medical Inc. on July 18, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1060039
- Company Name: Forge Medical Inc.
- Inspection Date: 2018-07-18
- 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 1205082 - 2023-04-18](https://www.keypedia.com/records/fda_inspections/forge-medical-inc/069c3058-9e26-44dc-b41b-280dbfe87d83)
- [FDA Inspection 1060039 - 2018-07-18](https://www.keypedia.com/records/fda_inspections/forge-medical-inc/30bae751-7f5b-4d2e-b619-b88905876543)

Company: https://www.keypedia.com/companies/forge-medical-inc/86a2ce8b-0b68-43bf-a3b2-de17c5a6a57b

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