# FDA Inspection 953841 - Starfish Product Engineering Inc. - December 11, 2015

Source: https://www.keypedia.com/records/fda_inspections/starfish-product-engineering-inc/1230f9e3-8db5-4f1c-8071-c1d398a6895c
Source feed: FDA_Inspections

> FDA Inspection 953841 for Starfish Product Engineering Inc. on December 11, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 953841
- Company Name: Starfish Product Engineering Inc.
- Inspection Date: 2015-12-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/starfish-product-engineering-inc/c04c293f-114c-49a3-b51a-bc3e32c12db1

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