# FDA Inspection 1034315 - Keystone Industries - Myerstown - July 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/keystone-industries-myerstown/2279f912-5d26-4fef-8043-4f8670904214
Source feed: FDA_Inspections

> FDA Inspection 1034315 for Keystone Industries - Myerstown on July 27, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1034315
- Company Name: Keystone Industries - Myerstown
- Inspection Date: 2017-07-27
- 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 1034315 - 2017-07-27](https://www.keypedia.com/records/fda_inspections/keystone-industries-myerstown/5dcc4763-9520-415a-a683-43c6682606b4)

Company: https://www.keypedia.com/companies/keystone-industries-myerstown/753277f4-9534-41d1-9a54-3109b361392a

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