# FDA Inspection 1069112 - Composite Manufacturing, Inc - September 27, 2018

Source: https://www.keypedia.com/records/fda_inspections/composite-manufacturing-inc/a577d8f5-8163-46e6-91ce-e3b2712aed3c
Source feed: FDA_Inspections

> FDA Inspection 1069112 for Composite Manufacturing, Inc on September 27, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069112
- Company Name: Composite Manufacturing, Inc
- Inspection Date: 2018-09-27
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1069112 - 2018-09-27](https://www.keypedia.com/records/fda_inspections/composite-manufacturing-inc/992093f4-6c15-49fd-b942-7f387938cb9d)
- [FDA Inspection 880903 - 2014-05-29](https://www.keypedia.com/records/fda_inspections/composite-manufacturing-inc/472ba9f5-1843-4113-a7d7-ed8a08f0f6be)

Company: https://www.keypedia.com/companies/composite-manufacturing-inc/39730b57-e24b-4edd-9135-6cf075c8c792

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