# Lcr-hallcrest, Llc. – FDA Inspection, Jan 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/lcr-hallcrest-llc/9c628486-6c26-483e-8ff9-88d4c7705b5c
Source feed: FDA_Inspections

> FDA inspection 1001750 of Lcr-hallcrest, Llc., January 27, 2017. Classification: Voluntary Action Indicated (VAI). 2 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: 1001750
- Company Name: Lcr-hallcrest, Llc.
- Inspection Date: 2017-01-27
- 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: 2

## Related Documents

- FDA Inspection 883371 - 2014-06-12
- [FDA Inspection 649662 - 2010-02-26](https://www.keypedia.com/records/fda_inspections/lcr-hallcrest-llc/beabc8d9-5b2a-4341-99b2-eee4c16b7243)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

Company: https://www.keypedia.com/companies/lcr-hallcrest-llc/2f71a684-79fa-4634-a330-845921d21978

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