FDA Inspection 1032159 — ME Center (Nagaizumi) Of Terumo Corp
The FDA completed an inspection of ME Center (Nagaizumi) Of Terumo Corp on Nov 2, 2017 in Sunto-Gun. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Nov 2, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sunto-Gun (Japan)
Citations
| ID | CFR | Description |
|---|---|---|
| 3313 | 21 CFR 820.120(d) | Records, DHR {see also 820.184(e)} |