# FDA Inspection 1016062 - Ondine Research Laboratories, Inc. - June 08, 2017

Source: https://www.keypedia.com/records/fda_inspections/ondine-research-laboratories-inc/f3d672f3-797b-4ef2-8386-e7ff87bb0dda
Source feed: FDA_Inspections

> FDA Inspection 1016062 for Ondine Research Laboratories, Inc. on June 08, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016062
- Company Name: Ondine Research Laboratories, Inc.
- Inspection Date: 2017-06-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1016062 - 2017-06-08](https://www.keypedia.com/records/fda_inspections/ondine-research-laboratories-inc/bb2dd5ea-c52a-453a-bfc8-d429c35931cc)
- [FDA Inspection 655208 - 2010-03-16](https://www.keypedia.com/records/fda_inspections/ondine-research-laboratories-inc/cd716d06-7dc0-4f67-ad03-7ecfa09df774)

Company: https://www.keypedia.com/companies/ondine-research-laboratories-inc/bd17c0a4-8381-429d-a5b9-460ddfb90bb9

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