# FDA Inspection 1060866 - Universal Orlando Resort - May 01, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/universal-orlando-resort/b79e7358-676f-443a-924a-95600fa6c2c1
Source feed: FDA_Inspections

> FDA Inspection 1060866 for Universal Orlando Resort on May 01, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1060866
- Company Name: Universal Orlando Resort
- Inspection Date: 2018-05-01
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 825749 - 2013-03-25](https://www.globalkeysolutions.net/records/fda_inspections/universal-orlando-resort/cd801f15-c32c-4cc2-8e9c-e1d00b320145)

Company: https://www.globalkeysolutions.net/companies/universal-orlando-resort/ad921fae-204f-4605-a6b4-1fa6337b034c

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