# Angstrom Mfg Inc – FDA Inspection, Aug 12, 2026

Source: https://www.keypedia.com/records/fda_inspections/angstrom-mfg-inc/d4701199-ce95-4678-b148-de2bb4e1efff
Source feed: FDA_Inspections

> FDA inspection 1330686 of Angstrom Mfg Inc, August 12, 2026. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 830. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1330686
- Company Name: Angstrom Mfg Inc
- Inspection Date: 2026-08-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 994001 - 2016-11-17
- [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