FDA Inspection 1075004 — Gregory Manufacturing, Inc.
The FDA completed an inspection of Gregory Manufacturing, Inc. on November 21, 2018 in Holyoke, MA. 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
- November 21, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Holyoke, MA (United States)