# FDA Inspection 774342 - Guenter Enderle Enterprises, Inc. Nekton USA - March 27, 2012

Source: https://www.keypedia.com/records/fda_inspections/guenter-enderle-enterprises-inc-nekton-usa/cbd622d7-6904-4c2a-bef7-35a1554d2efc
Source feed: FDA_Inspections

> FDA Inspection 774342 for Guenter Enderle Enterprises, Inc. Nekton USA on March 27, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 774342
- Company Name: Guenter Enderle Enterprises, Inc. Nekton USA
- Inspection Date: 2012-03-27
- Classification: No Action Indicated (NAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 774342 - 2012-03-27](https://www.keypedia.com/records/fda_inspections/guenter-enderle-enterprises-inc-nekton-usa/24083357-9b30-486d-8294-a5776eaa9299)

Company: https://www.keypedia.com/companies/guenter-enderle-enterprises-inc-nekton-usa/902c3bae-9cc2-49fe-a965-1182168b4a60

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c