# FDA Inspection 1101677 - BD - August 07, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/bd/ccad32f6-5eec-4601-978b-717300ed084f
Source feed: FDA_Inspections

> FDA Inspection 1101677 for BD on August 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1101677
- Company Name: BD
- Inspection Date: 2019-08-07
- 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 1101677 - 2019-08-07](https://www.globalkeysolutions.net/records/fda_inspections/bd/396e45e5-d3e0-4563-b345-0f2118e0c77b)
- [FDA Inspection 866686 - 2014-01-31](https://www.globalkeysolutions.net/records/fda_inspections/bd/fd72d41f-41ce-4ba4-8e95-8a47cf750f30)

Company: https://www.globalkeysolutions.net/companies/bd/072104d3-4324-4a12-a253-874a90bee3c0

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