# FDA Inspection 997471 - Suretex Prophylactics (India) Limited - December 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/suretex-prophylactics-india-limited/0779eddb-f2bb-4254-994c-4a44e4550dc2
Source feed: FDA_Inspections

> FDA Inspection 997471 for Suretex Prophylactics (India) Limited on December 21, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 997471
- Company Name: Suretex Prophylactics (India) Limited
- Inspection Date: 2016-12-21
- 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 997471 - 2016-12-21](https://www.keypedia.com/records/fda_inspections/suretex-prophylactics-india-limited/b02584a3-69bc-4757-94dd-5cc97f7d3225)
- [FDA Inspection 677767 - 2010-06-23](https://www.keypedia.com/records/fda_inspections/suretex-prophylactics-india-limited/94c40d26-1311-434c-b396-7976e7de9169)

Company: https://www.keypedia.com/companies/suretex-prophylactics-india-limited/cdce9b76-30c8-4005-8ab2-1d165c64b947

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