# FDA Inspection 830531 - SurgiMark, Inc. - May 02, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/surgimark-inc/fcbfad27-f95a-44c2-aec6-16dd2dc2ddd3/
Source feed: FDA_Inspections

> FDA Inspection 830531 for SurgiMark, Inc. on May 02, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 830531
- Company Name: SurgiMark, Inc.
- Inspection Date: 2013-05-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1023279 - 2017-08-08](https://www.globalkeysolutions.net/api/records/fda_inspections/surgimark-inc/5d8ff067-100a-417e-a5dd-ff7f52ba7072/)
- [FDA Inspection 1023279 - 2017-08-08](https://www.globalkeysolutions.net/api/records/fda_inspections/surgimark-inc/ab0dd42b-339a-435f-b09e-a2a11264ceb7/)
- [FDA Inspection 830531 - 2013-05-02](https://www.globalkeysolutions.net/api/records/fda_inspections/surgimark-inc/7b9316a9-223e-4fbc-ad2c-ad2236c9099f/)

Company: https://www.globalkeysolutions.net/companies/surgimark-inc/2ddd33d7-2d24-46ae-8d24-094fdcd20020

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