# FDA Inspection 860311 - CDR Manufacturing Inc. - January 07, 2014

Source: https://www.keypedia.com/records/fda_inspections/cdr-manufacturing-inc/a2b188ea-ace5-48d3-96f7-12ded2ed4c61
Source feed: FDA_Inspections

> FDA Inspection 860311 for CDR Manufacturing Inc. on January 07, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 860311
- Company Name: CDR Manufacturing Inc.
- Inspection Date: 2014-01-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/cdr-manufacturing-inc/c3ad8620-2404-425d-ab91-c1bf6278a0ab

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