# Angstrom Mfg Inc – FDA Inspection, Jun 8, 2011

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

> FDA inspection 729505 of Angstrom Mfg Inc, June 08, 2011. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 729505
- Company Name: Angstrom Mfg Inc
- Inspection Date: 2011-06-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1330686 - 2026-08-12](https://www.keypedia.com/records/fda_inspections/angstrom-mfg-inc/d4701199-ce95-4678-b148-de2bb4e1efff)
- FDA Inspection 994001 - 2016-11-17

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