# FDA Inspection 1087615 - CDR Manufacturing Inc. - March 26, 2019

Source: https://www.keypedia.com/records/fda_inspections/cdr-manufacturing-inc/950044b7-c62a-403e-ab2a-e7e2eb51bd1a
Source feed: FDA_Inspections

> FDA Inspection 1087615 for CDR Manufacturing Inc. on March 26, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1087615
- Company Name: CDR Manufacturing Inc.
- Inspection Date: 2019-03-26
- Classification: No Action Indicated (NAI)
- 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