# FDA Inspection 848201 - Drynite - August 23, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/drynite/41068c60-7cc9-4bea-b045-eb3242b2e759
Source feed: FDA_Inspections

> FDA Inspection 848201 for Drynite on August 23, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 848201
- Company Name: Drynite
- Inspection Date: 2013-08-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1079216 - 2018-12-04](https://www.globalkeysolutions.net/records/fda_inspections/drynite/cda3afd1-a35c-4695-b570-83b466248669)
- [FDA Inspection 848201 - 2013-08-23](https://www.globalkeysolutions.net/records/fda_inspections/drynite/56a6ea15-aa71-47d5-bbfe-95d13b054a84)

Company: https://www.globalkeysolutions.net/companies/drynite/2f31b0a1-6a37-4c05-b34c-cd3dc9070b48

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