FDA Inspection
Angstrom Mfg IncAngstrom Mfg Inc – FDA Inspection, Jun 8, 2011
Record Details
This FDA Inspection record concerns Angstrom Mfg Inc, with an inspection on June 8, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Angstrom Mfg Inc
- Inspection Date
- June 8, 2011
- Product Type
- Devices
View Company Profile
ID · b11d5617-2438-451c-9f91-1ec19be3bf9d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 729505
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.22Quality audits - Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.20(c)Management review dates
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Other FDA inspections of Angstrom Mfg Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 12, 2026 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 17, 2016 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Angstrom Mfg Inc
- FDA Inspection 1330686 - 2026-08-12
- FDA Inspection 994001 - 2016-11-17
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