# FDA Inspection 914308 - Interlab S.r.l. - January 29, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/interlab-srl/1c6b5bed-40ea-4670-8e45-07e22ab8c441
Source feed: FDA_Inspections

> FDA Inspection 914308 for Interlab S.r.l. on January 29, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 914308
- Company Name: Interlab S.r.l.
- Inspection Date: 2015-01-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 914308 - 2015-01-29](https://www.globalkeysolutions.net/records/fda_inspections/interlab-srl/38cfcf5c-bc36-4237-9622-ee7aa0d2ecfb)
- [FDA Inspection 806255 - 2012-10-25](https://www.globalkeysolutions.net/records/fda_inspections/interlab-srl/f5be514b-4821-4b43-8874-f2314e9715c6)
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Company: https://www.globalkeysolutions.net/companies/interlab-srl/1321253a-13bb-4306-a943-8d86bb259bf1

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7