# ActiTech, LP – FDA Inspection, May 24, 2010

Source: https://www.keypedia.com/records/fda_inspections/actitech-lp/628956ea-d5bb-45f1-a865-01707e7ba1b6
Source feed: FDA_Inspections

> FDA inspection 663582 of ActiTech, LP, May 24, 2010. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 211. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 663582
- Company Name: ActiTech, LP
- Inspection Date: 2010-05-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 3

## Related Documents

- FDA Inspection 1105208 - 2019-09-25
- FDA Inspection 749662 - 2011-08-23
- FDA Inspection 570526 - 2009-03-13

Company: https://www.keypedia.com/companies/actitech-lp/6a6e0ec6-9371-4fe6-88e5-53bdab1f3c8e

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