FDA Inspection 1098911 — LUBRINOVATION, Inc.
The FDA completed an inspection of LUBRINOVATION, Inc. on Aug 7, 2019 in Frederick, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 7, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Frederick, MD (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3117 | 21 CFR 820.70(i) | Software validation for automated processes |
| 479 | 21 CFR 820.50 | Purchasing controls, Lack of or inadequate procedures |