FDA Inspection 1007613 — Direx Systems Corp.
The FDA completed an inspection of Direx Systems Corp. on April 12, 2017 in Canton, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- April 12, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Canton, MA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3409 | 21 CFR 820.200(d) | Service reports |