# FDA Inspection 877783 - Futuremed America Inc - May 07, 2014

Source: https://www.keypedia.com/records/fda_inspections/futuremed-america-inc/a4e58ea6-8e22-48b3-a775-5b5a965f80df
Source feed: FDA_Inspections

> FDA Inspection 877783 for Futuremed America Inc on May 07, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 877783
- Company Name: Futuremed America Inc
- Inspection Date: 2014-05-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 786089 - 2012-05-29](https://www.keypedia.com/records/fda_inspections/futuremed-america-inc/39d764c3-7a88-4b15-8f0d-dda17bebe94a)
- [FDA Inspection 651858 - 2010-03-10](https://www.keypedia.com/records/fda_inspections/futuremed-america-inc/5199e8de-eb12-4410-8d4c-faf92053304a)
- [FDA Inspection 563821 - 2009-02-12](https://www.keypedia.com/records/fda_inspections/futuremed-america-inc/07733f6b-a406-419b-b35f-e12f063c1134)

Company: https://www.keypedia.com/companies/futuremed-america-inc/aa767cdd-02e7-4c07-959e-ce0b7323ab31

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