# FDA Inspection 1056202 - Procedure Products, Inc. - June 07, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/84a2e75d-b373-4647-bd59-40b2509788b3
Source feed: FDA_Inspections

> FDA Inspection 1056202 for Procedure Products, Inc. on June 07, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1056202
- Company Name: Procedure Products, Inc.
- Inspection Date: 2018-06-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1056202 - 2018-06-07](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/dd7f3968-b095-457d-b141-f0ec319bf05e)
- [FDA Inspection 908610 - 2015-01-05](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/d05d79eb-0c22-406e-8e59-fb5c95676736)
- [FDA Inspection 908610 - 2015-01-05](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/0d19a56d-a1d9-4694-b0a5-24ad581ea07a)
- [FDA Inspection 799630 - 2012-08-30](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/aeb1ab39-c1f0-4ad2-aad9-88a1b6e59e6d)
- [FDA Inspection 799630 - 2012-08-30](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/714bfbce-41a9-4224-91cb-72f3333f4bd2)

Company: https://www.globalkeysolutions.net/companies/procedure-products-inc/7fd29bd7-1dee-4c43-8b80-d6678a4c6d81

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