# FDA Inspection 950172 - Chandler Industries- Arrow Division - November 12, 2015

Source: https://www.keypedia.com/records/fda_inspections/chandler-industries-arrow-division/e96532b4-ab57-4235-a743-92eb5e7961d9
Source feed: FDA_Inspections

> FDA Inspection 950172 for Chandler Industries- Arrow Division on November 12, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 950172
- Company Name: Chandler Industries- Arrow Division
- Inspection Date: 2015-11-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 950172 - 2015-11-12](https://www.keypedia.com/records/fda_inspections/chandler-industries-arrow-division/8d9847df-9f3a-46e6-b849-be9b45ffe069)

Company: https://www.keypedia.com/companies/chandler-industries-arrow-division/483de5c6-f8b6-4780-849e-d18b485b5dac

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