FDA Inspection 994001 — Angstrom Mfg Inc
The FDA completed an inspection of Angstrom Mfg Inc on November 17, 2016 in Sainte Genevieve, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 17, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Sainte Genevieve, MO (United States)