# FDA Inspection 814049 - Proact Ltd - January 15, 2013

Source: https://www.keypedia.com/records/fda_inspections/proact-ltd/539a7cd9-6f96-42f5-bb3f-cd3b3679e737
Source feed: FDA_Inspections

> FDA Inspection 814049 for Proact Ltd on January 15, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 814049
- Company Name: Proact Ltd
- Inspection Date: 2013-01-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1107078 - 2019-09-12](https://www.keypedia.com/records/fda_inspections/proact-ltd/4d995a9c-40a7-410c-97f8-10c46c558ed1)

Company: https://www.keypedia.com/companies/proact-ltd/2e34c36b-ade7-450b-831b-ffb79bc20c68

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