# FDA Inspection 729505 - Angstrom Mfg Inc - June 08, 2011

Source: https://www.keypedia.com/records/fda_inspections/angstrom-mfg-inc/b11d5617-2438-451c-9f91-1ec19be3bf9d
Source feed: FDA_Inspections

> FDA Inspection 729505 for Angstrom Mfg Inc on June 08, 2011. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 729505
- Company Name: Angstrom Mfg Inc
- Inspection Date: 2011-06-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 994001 - 2016-11-17](https://www.keypedia.com/records/fda_inspections/angstrom-mfg-inc/464c7ef8-0fb1-474c-974a-e2b03a4a7735)
- [FDA Inspection 994001 - 2016-11-17](https://www.keypedia.com/records/fda_inspections/angstrom-mfg-inc/1fffece4-e0f6-4552-bb9f-870765a6249b)
- [FDA Inspection 994001 - 2016-11-17](https://www.keypedia.com/records/fda_inspections/angstrom-mfg-inc/c21683f1-d81b-4ae5-9864-fd63e35bb312)

Company: https://www.keypedia.com/companies/angstrom-mfg-inc/44e5c597-fd91-4b7a-91d7-308e48ccee00

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