# FDA Inspection 1223256 - StrongHold Group - October 31, 2023

Source: https://www.keypedia.com/records/fda_inspections/stronghold-group/549027cc-5e44-4629-a7ff-3402e7efeb7d
Source feed: FDA_Inspections

> FDA Inspection 1223256 for StrongHold Group on October 31, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1223256
- Company Name: StrongHold Group
- Inspection Date: 2023-10-31
- 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 1223256 - 2023-10-31](https://www.keypedia.com/records/fda_inspections/stronghold-group/e9706347-1f30-4b37-a841-53a7a7b462bf)

Company: https://www.keypedia.com/companies/stronghold-group/ff5ea046-415e-4aa1-8208-a5988eaff3f4

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