FDA Inspection 1156389 — Tecan CDMO Solutions MH, Corp

Tecan CDMO Solutions MH, Corp — FEI 3003537036

The FDA completed an inspection of Tecan CDMO Solutions MH, Corp on October 29, 2021 in Morgan Hill, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 29, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Morgan Hill, CA (United States)