# FDA Inspection 1201730 - ROM Technologies, Inc. - April 04, 2023

Source: https://www.keypedia.com/records/fda_inspections/rom-technologies-inc/d12b5b65-8f81-48eb-b789-add08c0720b9
Source feed: FDA_Inspections

> FDA Inspection 1201730 for ROM Technologies, Inc. on April 04, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1201730
- Company Name: ROM Technologies, Inc.
- Inspection Date: 2023-04-04
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/rom-technologies-inc/f395f198-c33e-4058-bde6-d341b920c02c

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