# FDA Inspection 850016 - Acro Biotech Inc. - September 03, 2013

Source: https://www.keypedia.com/records/fda_inspections/acro-biotech-inc/1c7cf068-b38e-4f6e-94b9-b9e5855be663
Source feed: FDA_Inspections

> FDA Inspection 850016 for Acro Biotech Inc. on September 03, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 850016
- Company Name: Acro Biotech Inc.
- Inspection Date: 2013-09-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1050458 - 2018-05-01](https://www.keypedia.com/records/fda_inspections/acro-biotech-inc/cff77bf3-b41f-45a9-9283-85a0a321bc8f)
- [FDA Inspection 1050458 - 2018-05-01](https://www.keypedia.com/records/fda_inspections/acro-biotech-inc/88e89679-6327-4f26-ae49-47c8d119ab7f)
- [FDA Inspection 850016 - 2013-09-03](https://www.keypedia.com/records/fda_inspections/acro-biotech-inc/e82a2a58-2a38-42b5-98d8-a1f646a53b21)

Company: https://www.keypedia.com/companies/acro-biotech-inc/2591a2ab-9c6e-49ca-8e26-ee9988a22eb5

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