# CDR Manufacturing Inc. – FDA Inspection, Jan 7, 2014

Source: https://www.keypedia.com/records/fda_inspections/cdr-manufacturing-inc/a6b18e81-f1fd-4841-8bcb-0ec5c81fb886
Source feed: FDA_Inspections

> FDA inspection 860311 of CDR Manufacturing Inc., January 07, 2014. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1197245 - 2023-02-02
- FDA Inspection 1087615 - 2019-03-26

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