FDA Inspection 897353 — The EF Precision Group
The FDA completed an inspection of The EF Precision Group on September 25, 2014 in Willow Grove, PA. 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
- September 25, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Willow Grove, PA (United States)