# Control Devices - Carr Lane – FDA Inspection, Mar 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/control-devices-carr-lane/79f852e9-3893-413a-8b70-6b18cd01f6df
Source feed: FDA_Inspections

> FDA inspection 1009753 of Control Devices - Carr Lane, March 28, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1009753
- Company Name: Control Devices - Carr Lane
- Inspection Date: 2017-03-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 832345 - 2013-05-15
- FDA Inspection 611151 - 2009-09-14

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/eric-m-padgett/a42150bc-aa7f-4076-8a68-af47ff465bac)

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