# FDA Inspection 1009753 - Control Devices - Carr Lane - March 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/control-devices-carr-lane/14b2c6e9-3c6b-4cf3-bf00-922dde805473
Source feed: FDA_Inspections

> FDA Inspection 1009753 for Control Devices - Carr Lane on March 28, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1009753
- Company Name: Control Devices - Carr Lane
- Inspection Date: 2017-03-28
- 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 1009753 - 2017-03-28](https://www.keypedia.com/records/fda_inspections/control-devices-carr-lane/79f852e9-3893-413a-8b70-6b18cd01f6df)
- [FDA Inspection 832345 - 2013-05-15](https://www.keypedia.com/records/fda_inspections/control-devices-carr-lane/8b0e162b-1083-4c29-83f6-41f2ca5e5ac1)
- [FDA Inspection 611151 - 2009-09-14](https://www.keypedia.com/records/fda_inspections/control-devices-carr-lane/204cb167-c5c1-4998-a9bf-92e9c7a792b7)

Company: https://www.keypedia.com/companies/control-devices-carr-lane/aec3937c-c223-4892-8b0b-e0a02cc578f6

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