# FDA Inspection 994001 - Angstrom Mfg Inc - November 17, 2016

Source: https://www.keypedia.com/records/fda_inspections/angstrom-mfg-inc/464c7ef8-0fb1-474c-974a-e2b03a4a7735
Source feed: FDA_Inspections

> FDA Inspection 994001 for Angstrom Mfg Inc on November 17, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 994001
- Company Name: Angstrom Mfg Inc
- Inspection Date: 2016-11-17
- Classification: No Action Indicated (NAI)
- 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/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)
- [FDA Inspection 729505 - 2011-06-08](https://www.keypedia.com/records/fda_inspections/angstrom-mfg-inc/b11d5617-2438-451c-9f91-1ec19be3bf9d)

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