FDA Inspection 740152 — Willy Rusch GmbH A Div Of Teleflex Medical
The FDA completed an inspection of Willy Rusch GmbH A Div Of Teleflex Medical on Jul 21, 2011 in Kernen Im Remstal. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jul 21, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Kernen Im Remstal (Germany)
Citations
| ID | CFR | Description |
|---|---|---|
| 3159 | 21 CFR 820.184 | DHR content |