# FDA Inspection 1064636 - Strauman Manufacturing Inc. - August 30, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/strauman-manufacturing-inc/4a51c5d9-738c-410c-9b8f-18182a09da13
Source feed: FDA_Inspections

> FDA Inspection 1064636 for Strauman Manufacturing Inc. on August 30, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1064636
- Company Name: Strauman Manufacturing Inc.
- Inspection Date: 2018-08-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1064636 - 2018-08-30](https://www.globalkeysolutions.net/records/fda_inspections/strauman-manufacturing-inc/449bb278-29e1-469b-83a3-224a5abb5e38)

Company: https://www.globalkeysolutions.net/companies/strauman-manufacturing-inc/8ee6e0e9-f3e3-433d-b14c-6899678e4c84

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