# FDA Inspection 840804 - Brooklands, Inc. - July 23, 2013

Source: https://www.keypedia.com/records/fda_inspections/brooklands-inc/614f0cca-cbf0-45d5-adaf-4b50ab5abd20
Source feed: FDA_Inspections

> FDA Inspection 840804 for Brooklands, Inc. on July 23, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 840804
- Company Name: Brooklands, Inc.
- Inspection Date: 2013-07-23
- 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 840804 - 2013-07-23](https://www.keypedia.com/records/fda_inspections/brooklands-inc/cb433069-a4e2-48ff-a262-07f0bc6ec152)
- [FDA Inspection 800940 - 2012-09-14](https://www.keypedia.com/records/fda_inspections/brooklands-inc/73ddb878-51ce-420d-bea2-c53103dd5181)
- [FDA Inspection 800940 - 2012-09-14](https://www.keypedia.com/records/fda_inspections/brooklands-inc/63b596fe-e356-4159-985b-1606b591078a)

Company: https://www.keypedia.com/companies/brooklands-inc/f5ef77d5-3435-431d-9e1f-f541d4d2746c

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